Canonical Allele Identifier: CA1607949764

Gene: F13A1

Linked Data

• dbSNP Id: rs1583041027
• gnomAD v4: 6-6145539-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6145539G>A , CM000668.2:g.6145539G>A	GRCh38
NC_000006.11:g.6145772G>A , CM000668.1:g.6145772G>A	GRCh37
NC_000006.10:g.6090771G>A	NCBI36
NG_008107.1:g.180153C>T , LRG_549:g.180153C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264870.8:c.*80C>T MANE Select	ENSP00000264870.3:n.*80C>T
ENST00000264870.7:c.*80C>T	ENSP00000264870.3:n.*80C>T
NM_000129.3:c.*80C>T , LRG_549t1:c.*80C>T	NP_000120.2:n.*80C>T
XM_006715010.2:c.*80C>T	XP_006715073.1:n.*80C>T
XM_011514342.1:c.*80C>T	XP_011512644.1:n.*80C>T
NM_000129.4:c.*80C>T MANE Select	NP_000120.2:n.*80C>T