Canonical Allele Identifier: CA1139953650
Gene: SERPINC1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173904221T= , CM000663.2:g.173904221T= GRCh38
NC_000001.10:g.173873359T= , CM000663.1:g.173873359T= GRCh37
NC_000001.9:g.172139982T= NCBI36
NG_012462.1:g.18158A= , LRG_577:g.18158A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1219-156A= MANE Select ENSP00000356671.3:n.1219-156A=
ENST00000367698.3:c.1219-156A= ENSP00000356671.3:n.1219-156A=
ENST00000617423.4:c.604-156A= ENSP00000478688.1:n.604-156A=
NM_000488.3:c.1219-156A= , LRG_577t1:c.1219-156A= NP_000479.1:n.1219-156A=
XM_005245198.2:c.1075-156A= XP_005245255.1:n.1075-156A=
NM_001365052.1:c.1075-156A= NP_001351981.1:n.1075-156A=
NM_000488.4:c.1219-156A= MANE Select NP_000479.1:n.1219-156A=
NM_001365052.2:c.1075-156A= NP_001351981.1:n.1075-156A=
NM_001386302.1:c.1342-156A= NP_001373231.1:n.1342-156A=
NM_001386303.1:c.1300-156A= NP_001373232.1:n.1300-156A=
NM_001386304.1:c.1198-156A= NP_001373233.1:n.1198-156A=
NM_001386305.1:c.1162-156A= NP_001373234.1:n.1162-156A=
NM_001386306.1:c.1003-156A= NP_001373235.1:n.1003-156A=
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