Canonical Allele Identifier: CA645847058

Gene: F13B

Linked Data

• COSMIC: COSN18725202 ; COSN18725219

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197039350_197039351insG , CM000663.2:g.197039350_197039351insG	GRCh38
NC_000001.10:g.197008480_197008481insG , CM000663.1:g.197008480_197008481insG	GRCh37
NC_000001.9:g.195275103_195275104insG	NCBI36
NG_012065.1:g.32917_32918insC , LRG_550:g.32917_32918insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367412.2:c.*27_*28insC MANE Select	ENSP00000356382.2:n.*27_*28insC
ENST00000649282.1:c.768_769insC	ENSP00000497116.1:n.768_769insC
ENST00000367412.1:c.*27_*28insC	ENSP00000356382.1:n.*27_*28insC
NM_001994.2:c.*27_*28insC , LRG_550t1:c.*27_*28insC	NP_001985.2:n.*27_*28insC
XM_011509283.2:c.*948_*949insC	XP_011507585.1:n.*948_*949insC
XM_011509284.2:c.*948_*949insC	XP_011507586.1:n.*948_*949insC
XM_011509286.2:c.*948_*949insC	XP_011507588.1:n.*948_*949insC
NM_001994.3:c.*27_*28insC MANE Select	NP_001985.2:n.*27_*28insC