Canonical Allele Identifier: CA2677189476
Gene: F13A1 HGNC NCBI

Linked Data

gnomAD v4: 6-6145359-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6145359T>A , CM000668.2:g.6145359T>A GRCh38
NC_000006.11:g.6145592T>A , CM000668.1:g.6145592T>A GRCh37
NC_000006.10:g.6090591T>A NCBI36
NG_008107.1:g.180333A>T , LRG_549:g.180333A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264870.8:c.*260A>T MANE Select ENSP00000264870.3:n.*260A>T
ENST00000264870.7:c.*260A>T ENSP00000264870.3:n.*260A>T
NM_000129.3:c.*260A>T , LRG_549t1:c.*260A>T NP_000120.2:n.*260A>T
XM_006715010.2:c.*260A>T XP_006715073.1:n.*260A>T
XM_011514342.1:c.*260A>T XP_011512644.1:n.*260A>T
NM_000129.4:c.*260A>T MANE Select NP_000120.2:n.*260A>T