Canonical Allele Identifier: CA343772042
Gene: SERPINC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903903G>T , CM000663.2:g.173903903G>T GRCh38
NC_000001.10:g.173873041G>T , CM000663.1:g.173873041G>T GRCh37
NC_000001.9:g.172139664G>T NCBI36
NG_012462.1:g.18476C>A , LRG_577:g.18476C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000367698.4:c.1381C>A MANE Select ENSP00000356671.3:p.Pro461Thr
ENST00000367698.3:c.1381C>A ENSP00000356671.3:p.Pro461Thr
ENST00000617423.4:c.766C>A ENSP00000478688.1:p.Pro256Thr
NM_000488.3:c.1381C>A , LRG_577t1:c.1381C>A NP_000479.1:p.Pro461Thr
XM_005245198.2:c.1237C>A XP_005245255.1:p.Pro413Thr
NM_001365052.1:c.1237C>A NP_001351981.1:p.Pro413Thr
NM_000488.4:c.1381C>A MANE Select NP_000479.1:p.Pro461Thr
NM_001365052.2:c.1237C>A NP_001351981.1:p.Pro413Thr
NM_001386302.1:c.1504C>A NP_001373231.1:p.Pro502Thr
NM_001386303.1:c.1462C>A NP_001373232.1:p.Pro488Thr
NM_001386304.1:c.1360C>A NP_001373233.1:p.Pro454Thr
NM_001386305.1:c.1324C>A NP_001373234.1:p.Pro442Thr
NM_001386306.1:c.1165C>A NP_001373235.1:p.Pro389Thr