Canonical Allele Identifier: CA1207936878
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909509A= , CM000663.2:g.173909509A= GRCh38
NC_000001.10:g.173878647A= , CM000663.1:g.173878647A= GRCh37
NC_000001.9:g.172145270A= NCBI36
NG_012462.1:g.12870T= , LRG_577:g.12870T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1153+43T= MANE Select ENSP00000356671.3:n.1153+43T=
ENST00000367698.3:c.1153+43T= ENSP00000356671.3:n.1153+43T=
ENST00000617423.4:c.560-2016T= ENSP00000478688.1:n.560-2016T=
NM_000488.3:c.1153+43T= , LRG_577t1:c.1153+43T= NP_000479.1:n.1153+43T=
XM_005245198.2:c.1009+43T= XP_005245255.1:n.1009+43T=
NM_001365052.1:c.1009+43T= NP_001351981.1:n.1009+43T=
NM_000488.4:c.1153+43T= MANE Select NP_000479.1:n.1153+43T=
NM_001365052.2:c.1009+43T= NP_001351981.1:n.1009+43T=
NM_001386302.1:c.1276+43T= NP_001373231.1:n.1276+43T=
NM_001386303.1:c.1234+43T= NP_001373232.1:n.1234+43T=
NM_001386304.1:c.1132+43T= NP_001373233.1:n.1132+43T=
NM_001386305.1:c.1096+43T= NP_001373234.1:n.1096+43T=
NM_001386306.1:c.937+43T= NP_001373235.1:n.937+43T=