Canonical Allele Identifier: CA2677189378

Gene: F13A1

Linked Data

• gnomAD v4: 6-6145287-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6145287C>A , CM000668.2:g.6145287C>A	GRCh38
NC_000006.11:g.6145520C>A , CM000668.1:g.6145520C>A	GRCh37
NC_000006.10:g.6090519C>A	NCBI36
NG_008107.1:g.180405G>T , LRG_549:g.180405G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264870.8:c.*332G>T MANE Select	ENSP00000264870.3:n.*332G>T
ENST00000264870.7:c.*332G>T	ENSP00000264870.3:n.*332G>T
NM_000129.3:c.*332G>T , LRG_549t1:c.*332G>T	NP_000120.2:n.*332G>T
XM_006715010.2:c.*332G>T	XP_006715073.1:n.*332G>T
XM_011514342.1:c.*332G>T	XP_011512644.1:n.*332G>T
NM_000129.4:c.*332G>T MANE Select	NP_000120.2:n.*332G>T