Canonical Allele Identifier: CA2677189686

Gene: F13A1

Linked Data

• gnomAD v4: 6-6145519-TCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6145523_6145524del , CM000668.2:g.6145523_6145524del	GRCh38
NC_000006.11:g.6145756_6145757del , CM000668.1:g.6145756_6145757del	GRCh37
NC_000006.10:g.6090755_6090756del	NCBI36
NG_008107.1:g.180171_180172del , LRG_549:g.180171_180172del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264870.8:c.*98_*99del MANE Select	ENSP00000264870.3:n.*98_*99del
ENST00000264870.7:c.*98_*99del	ENSP00000264870.3:n.*98_*99del
NM_000129.3:c.*98_*99del , LRG_549t1:c.*98_*99del	NP_000120.2:n.*98_*99del
XM_006715010.2:c.*98_*99del	XP_006715073.1:n.*98_*99del
XM_011514342.1:c.*98_*99del	XP_011512644.1:n.*98_*99del
NM_000129.4:c.*98_*99del MANE Select	NP_000120.2:n.*98_*99del