Canonical Allele Identifier: CA343772156
Gene: SERPINC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903928A>C , CM000663.2:g.173903928A>C GRCh38
NC_000001.10:g.173873066A>C , CM000663.1:g.173873066A>C GRCh37
NC_000001.9:g.172139689A>C NCBI36
NG_012462.1:g.18451T>G , LRG_577:g.18451T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1356T>G MANE Select ENSP00000356671.3:p.Ile452Met
ENST00000367698.3:c.1356T>G ENSP00000356671.3:p.Ile452Met
ENST00000617423.4:c.741T>G ENSP00000478688.1:p.Ile247Met
NM_000488.3:c.1356T>G , LRG_577t1:c.1356T>G NP_000479.1:p.Ile452Met
XM_005245198.2:c.1212T>G XP_005245255.1:p.Ile404Met
NM_001365052.1:c.1212T>G NP_001351981.1:p.Ile404Met
NM_000488.4:c.1356T>G MANE Select NP_000479.1:p.Ile452Met
NM_001365052.2:c.1212T>G NP_001351981.1:p.Ile404Met
NM_001386302.1:c.1479T>G NP_001373231.1:p.Ile493Met
NM_001386303.1:c.1437T>G NP_001373232.1:p.Ile479Met
NM_001386304.1:c.1335T>G NP_001373233.1:p.Ile445Met
NM_001386305.1:c.1299T>G NP_001373234.1:p.Ile433Met
NM_001386306.1:c.1140T>G NP_001373235.1:p.Ile380Met