Canonical Allele Identifier: CA1217904227

Gene: F13B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197039416_197039417delinsAG , CM000663.2:g.197039416_197039417delinsAG	GRCh38
NC_000001.10:g.197008546_197008547delinsAG , CM000663.1:g.197008546_197008547delinsAG	GRCh37
NC_000001.9:g.195275169_195275170delinsAG	NCBI36
NG_012065.1:g.32851_32852delinsCT , LRG_550:g.32851_32852delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000367412.2:c.1953-6_1953-5delinsCT MANE Select	ENSP00000356382.2:n.1953-6_1953-5delinsCT...
ENST00000649282.1:c.708-6_708-5delinsCT	ENSP00000497116.1:n.708-6_708-5delinsCT
ENST00000367412.1:c.1953-6_1953-5delinsCT	ENSP00000356382.1:n.1953-6_1953-5delinsCT...
NM_001994.2:c.1953-6_1953-5delinsCT , LRG_550t1:c.1953-6_1953-5delinsCT	NP_001985.2:n.1953-6_1953-5delinsCT
XM_011509283.2:c.*882_*883delinsCT	XP_011507585.1:n.*882_*883delinsCT
XM_011509284.2:c.*882_*883delinsCT	XP_011507586.1:n.*882_*883delinsCT
XM_011509286.2:c.*882_*883delinsCT	XP_011507588.1:n.*882_*883delinsCT
NM_001994.3:c.1953-6_1953-5delinsCT MANE Select	NP_001985.2:n.1953-6_1953-5delinsCT