Canonical Allele Identifier: CA2769867644

Gene: F13A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6145561_6145562insTTTT , CM000668.2:g.6145561_6145562insTTTT	GRCh38
NC_000006.11:g.6145794_6145795insTTTT , CM000668.1:g.6145794_6145795insTTTT	GRCh37
NC_000006.10:g.6090793_6090794insTTTT	NCBI36
NG_008107.1:g.180133_180134insAAAA , LRG_549:g.180133_180134insAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264870.8:c.*60_*61insAAAA MANE Select	ENSP00000264870.3:n.*60_*61insAAAA
ENST00000264870.7:c.*60_*61insAAAA	ENSP00000264870.3:n.*60_*61insAAAA
NM_000129.3:c.*60_*61insAAAA , LRG_549t1:c.*60_*61insAAAA	NP_000120.2:n.*60_*61insAAAA
XM_006715010.2:c.*60_*61insAAAA	XP_006715073.1:n.*60_*61insAAAA
XM_011514342.1:c.*60_*61insAAAA	XP_011512644.1:n.*60_*61insAAAA
NM_000129.4:c.*60_*61insAAAA MANE Select	NP_000120.2:n.*60_*61insAAAA