Canonical Allele Identifier: CA1207937111
Gene: SERPINC1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173910071A= , CM000663.2:g.173910071A= GRCh38
NC_000001.10:g.173879209A= , CM000663.1:g.173879209A= GRCh37
NC_000001.9:g.172145832A= NCBI36
NG_012462.1:g.12308T= , LRG_577:g.12308T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.763-129T= MANE Select ENSP00000356671.3:n.763-129T=
ENST00000367698.3:c.763-129T= ENSP00000356671.3:n.763-129T=
ENST00000487183.1:n.414-129T=
ENST00000617423.4:c.559+1793T= ENSP00000478688.1:n.559+1793T=
NM_000488.3:c.763-129T= , LRG_577t1:c.763-129T= NP_000479.1:n.763-129T=
XM_005245198.2:c.619-129T= XP_005245255.1:n.619-129T=
NM_001365052.1:c.619-129T= NP_001351981.1:n.619-129T=
NM_000488.4:c.763-129T= MANE Select NP_000479.1:n.763-129T=
NM_001365052.2:c.619-129T= NP_001351981.1:n.619-129T=
NM_001386302.1:c.886-129T= NP_001373231.1:n.886-129T=
NM_001386303.1:c.844-129T= NP_001373232.1:n.844-129T=
NM_001386304.1:c.742-129T= NP_001373233.1:n.742-129T=
NM_001386305.1:c.763-186T= NP_001373234.1:n.763-186T=
NM_001386306.1:c.547-129T= NP_001373235.1:n.547-129T=
Search 100 bp 5'
Search 100 bp 3'