Canonical Allele Identifier: CA343772381
Gene: SERPINC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903971C>G , CM000663.2:g.173903971C>G GRCh38
NC_000001.10:g.173873109C>G , CM000663.1:g.173873109C>G GRCh37
NC_000001.9:g.172139732C>G NCBI36
NG_012462.1:g.18408G>C , LRG_577:g.18408G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000367698.4:c.1313G>C MANE Select ENSP00000356671.3:p.Arg438Thr
ENST00000367698.3:c.1313G>C ENSP00000356671.3:p.Arg438Thr
ENST00000617423.4:c.698G>C ENSP00000478688.1:p.Arg233Thr
NM_000488.3:c.1313G>C , LRG_577t1:c.1313G>C NP_000479.1:p.Arg438Thr
XM_005245198.2:c.1169G>C XP_005245255.1:p.Arg390Thr
NM_001365052.1:c.1169G>C NP_001351981.1:p.Arg390Thr
NM_000488.4:c.1313G>C MANE Select NP_000479.1:p.Arg438Thr
NM_001365052.2:c.1169G>C NP_001351981.1:p.Arg390Thr
NM_001386302.1:c.1436G>C NP_001373231.1:p.Arg479Thr
NM_001386303.1:c.1394G>C NP_001373232.1:p.Arg465Thr
NM_001386304.1:c.1292G>C NP_001373233.1:p.Arg431Thr
NM_001386305.1:c.1256G>C NP_001373234.1:p.Arg419Thr
NM_001386306.1:c.1097G>C NP_001373235.1:p.Arg366Thr