Canonical Allele Identifier: CA2551841438

Gene: F13B

Linked Data

• gnomAD v4: 1-197039137-A-ATC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197039137_197039138insTC , CM000663.2:g.197039137_197039138insTC	GRCh38
NC_000001.10:g.197008267_197008268insTC , CM000663.1:g.197008267_197008268insTC	GRCh37
NC_000001.9:g.195274890_195274891insTC	NCBI36
NG_012065.1:g.33130_33131insGA , LRG_550:g.33130_33131insGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367412.2:c.*240_*241insGA MANE Select	ENSP00000356382.2:n.*240_*241insGA
ENST00000649282.1:c.981_982insGA	ENSP00000497116.1:n.981_982insGA
XM_011509283.2:c.*1161_*1162insGA	XP_011507585.1:n.*1161_*1162insGA
XM_011509284.2:c.*1161_*1162insGA	XP_011507586.1:n.*1161_*1162insGA
XM_011509286.2:c.*1161_*1162insGA	XP_011507588.1:n.*1161_*1162insGA
NM_001994.3:c.*240_*241insGA MANE Select	NP_001985.2:n.*240_*241insGA