Canonical Allele Identifier: CA2568296490

Gene: F13B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197039223_197039224insATATAC , CM000663.2:g.197039223_197039224insATATAC	GRCh38
NC_000001.10:g.197008353_197008354insATATAC , CM000663.1:g.197008353_197008354insATATAC	GRCh37
NC_000001.9:g.195274976_195274977insATATAC	NCBI36
NG_012065.1:g.33044_33045insGTATAT , LRG_550:g.33044_33045insGTATAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367412.2:c.*154_*155insGTATAT MANE Select	ENSP00000356382.2:n.*154_*155insGTATAT
ENST00000649282.1:c.895_896insGTATAT	ENSP00000497116.1:n.895_896insGTATAT
ENST00000367412.1:c.*154_*155insGTATAT	ENSP00000356382.1:n.*154_*155insGTATAT
NM_001994.2:c.*154_*155insGTATAT , LRG_550t1:c.*154_*155insGTATAT	NP_001985.2:n.*154_*155insGTATAT
XM_011509283.2:c.*1075_*1076insGTATAT	XP_011507585.1:n.*1075_*1076insGTATAT
XM_011509284.2:c.*1075_*1076insGTATAT	XP_011507586.1:n.*1075_*1076insGTATAT
XM_011509286.2:c.*1075_*1076insGTATAT	XP_011507588.1:n.*1075_*1076insGTATAT
NM_001994.3:c.*154_*155insGTATAT MANE Select	NP_001985.2:n.*154_*155insGTATAT