Canonical Allele Identifier: CA343772461
Gene: SERPINC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903984A>G , CM000663.2:g.173903984A>G GRCh38
NC_000001.10:g.173873122A>G , CM000663.1:g.173873122A>G GRCh37
NC_000001.9:g.172139745A>G NCBI36
NG_012462.1:g.18395T>C , LRG_577:g.18395T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000367698.4:c.1300T>C MANE Select ENSP00000356671.3:p.Phe434Leu
ENST00000367698.3:c.1300T>C ENSP00000356671.3:p.Phe434Leu
ENST00000617423.4:c.685T>C ENSP00000478688.1:p.Phe229Leu
NM_000488.3:c.1300T>C , LRG_577t1:c.1300T>C NP_000479.1:p.Phe434Leu
XM_005245198.2:c.1156T>C XP_005245255.1:p.Phe386Leu
NM_001365052.1:c.1156T>C NP_001351981.1:p.Phe386Leu
NM_000488.4:c.1300T>C MANE Select NP_000479.1:p.Phe434Leu
NM_001365052.2:c.1156T>C NP_001351981.1:p.Phe386Leu
NM_001386302.1:c.1423T>C NP_001373231.1:p.Phe475Leu
NM_001386303.1:c.1381T>C NP_001373232.1:p.Phe461Leu
NM_001386304.1:c.1279T>C NP_001373233.1:p.Phe427Leu
NM_001386305.1:c.1243T>C NP_001373234.1:p.Phe415Leu
NM_001386306.1:c.1084T>C NP_001373235.1:p.Phe362Leu