Canonical Allele Identifier: CA2711109257

Gene: F13A1

Linked Data

• dbSNP Id: rs2151066324

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6144950del , CM000668.2:g.6144950del	GRCh38
NC_000006.11:g.6145183del , CM000668.1:g.6145183del	GRCh37
NC_000006.10:g.6090182del	NCBI36
NG_008107.1:g.180742del , LRG_549:g.180742del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264870.8:c.*669del MANE Select	ENSP00000264870.3:n.*669del
ENST00000264870.7:c.*669del	ENSP00000264870.3:n.*669del
NM_000129.3:c.*669del , LRG_549t1:c.*669del	NP_000120.2:n.*669del
XM_006715010.2:c.*669del	XP_006715073.1:n.*669del
XM_011514342.1:c.*669del	XP_011512644.1:n.*669del
NM_000129.4:c.*669del MANE Select	NP_000120.2:n.*669del