Canonical Allele Identifier: CA1217904197

Gene: F13B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197039330_197039331delinsGA , CM000663.2:g.197039330_197039331delinsGA	GRCh38
NC_000001.10:g.197008460_197008461delinsGA , CM000663.1:g.197008460_197008461delinsGA	GRCh37
NC_000001.9:g.195275083_195275084delinsGA	NCBI36
NG_012065.1:g.32937_32938delinsTC , LRG_550:g.32937_32938delinsTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000367412.2:c.*47_*48delinsTC MANE Select	ENSP00000356382.2:n.*47_*48delinsTC
ENST00000649282.1:c.788_789delinsTC	ENSP00000497116.1:n.788_789delinsTC
ENST00000367412.1:c.*47_*48delinsTC	ENSP00000356382.1:n.*47_*48delinsTC
NM_001994.2:c.*47_*48delinsTC , LRG_550t1:c.*47_*48delinsTC	NP_001985.2:n.*47_*48delinsTC
XM_011509283.2:c.*968_*969delinsTC	XP_011507585.1:n.*968_*969delinsTC
XM_011509284.2:c.*968_*969delinsTC	XP_011507586.1:n.*968_*969delinsTC
XM_011509286.2:c.*968_*969delinsTC	XP_011507588.1:n.*968_*969delinsTC
NM_001994.3:c.*47_*48delinsTC MANE Select	NP_001985.2:n.*47_*48delinsTC