Canonical Allele Identifier: CA1217904146

Gene: F13B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197039161_197039163delinsCAA , CM000663.2:g.197039161_197039163delinsCAA	GRCh38
NC_000001.10:g.197008291_197008293delinsCAA , CM000663.1:g.197008291_197008293delinsCAA	GRCh37
NC_000001.9:g.195274914_195274916delinsCAA	NCBI36
NG_012065.1:g.33105_33107delinsTTG , LRG_550:g.33105_33107delinsTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367412.2:c.*215_*217delinsTTG MANE Select	ENSP00000356382.2:n.*215_*217delinsTTG
ENST00000649282.1:c.956_958delinsTTG	ENSP00000497116.1:n.956_958delinsTTG
XM_011509283.2:c.*1136_*1138delinsTTG	XP_011507585.1:n.*1136_*1138delinsTTG
XM_011509284.2:c.*1136_*1138delinsTTG	XP_011507586.1:n.*1136_*1138delinsTTG
XM_011509286.2:c.*1136_*1138delinsTTG	XP_011507588.1:n.*1136_*1138delinsTTG
NM_001994.3:c.*215_*217delinsTTG MANE Select	NP_001985.2:n.*215_*217delinsTTG