Canonical Allele Identifier: CA343772051
Gene: SERPINC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903905T>G , CM000663.2:g.173903905T>G GRCh38
NC_000001.10:g.173873043T>G , CM000663.1:g.173873043T>G GRCh37
NC_000001.9:g.172139666T>G NCBI36
NG_012462.1:g.18474A>C , LRG_577:g.18474A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000367698.4:c.1379A>C MANE Select ENSP00000356671.3:p.Asn460Thr
ENST00000367698.3:c.1379A>C ENSP00000356671.3:p.Asn460Thr
ENST00000617423.4:c.764A>C ENSP00000478688.1:p.Asn255Thr
NM_000488.3:c.1379A>C , LRG_577t1:c.1379A>C NP_000479.1:p.Asn460Thr
XM_005245198.2:c.1235A>C XP_005245255.1:p.Asn412Thr
NM_001365052.1:c.1235A>C NP_001351981.1:p.Asn412Thr
NM_000488.4:c.1379A>C MANE Select NP_000479.1:p.Asn460Thr
NM_001365052.2:c.1235A>C NP_001351981.1:p.Asn412Thr
NM_001386302.1:c.1502A>C NP_001373231.1:p.Asn501Thr
NM_001386303.1:c.1460A>C NP_001373232.1:p.Asn487Thr
NM_001386304.1:c.1358A>C NP_001373233.1:p.Asn453Thr
NM_001386305.1:c.1322A>C NP_001373234.1:p.Asn441Thr
NM_001386306.1:c.1163A>C NP_001373235.1:p.Asn388Thr