Canonical Allele Identifier: CA1608002829
Gene: F13A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6248337T= , CM000668.2:g.6248337T= GRCh38
NC_000006.11:g.6248570T= , CM000668.1:g.6248570T= GRCh37
NC_000006.10:g.6193569T= NCBI36
NG_008107.1:g.77355A= , LRG_549:g.77355A=

Transcript Alleles

HGVS Amino-acid change
ENST00000264870.8:c.773A= MANE Select ENSP00000264870.3:p.Lys258=
ENST00000264870.7:c.773A= ENSP00000264870.3:p.Lys258=
NM_000129.3:c.773A= , LRG_549t1:c.773A= NP_000120.2:p.Lys258=
XM_006715010.2:c.773A= XP_006715073.1:p.Lys258=
XM_011514342.1:c.935A= XP_011512644.1:p.Lys312=
NM_000129.4:c.773A= MANE Select NP_000120.2:p.Lys258=