Canonical Allele Identifier: CA2677189748

Gene: F13A1

Linked Data

• gnomAD v4: 6-6145606-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6145607dup , CM000668.2:g.6145607dup	GRCh38
NC_000006.11:g.6145840dup , CM000668.1:g.6145840dup	GRCh37
NC_000006.10:g.6090839dup	NCBI36
NG_008107.1:g.180085dup , LRG_549:g.180085dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264870.8:c.*12dup MANE Select	ENSP00000264870.3:n.*12dup
ENST00000264870.7:c.*12dup	ENSP00000264870.3:n.*12dup
NM_000129.3:c.*12dup , LRG_549t1:c.*12dup	NP_000120.2:n.*12dup
XM_006715010.2:c.*12dup	XP_006715073.1:n.*12dup
XM_011514342.1:c.*12dup	XP_011512644.1:n.*12dup
NM_000129.4:c.*12dup MANE Select	NP_000120.2:n.*12dup