Canonical Allele Identifier: CA6370042

Gene: JAM3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134144778_134144779insCTT , CM000673.2:g.134144778_134144779insCTT	GRCh38
NC_000011.9:g.134014673_134014674insCTT , CM000673.1:g.134014673_134014674insCTT	GRCh37
NC_000011.8:g.133519883_133519884insCTT	NCBI36
NG_028348.1:g.80854_80855insCTT

Transcript Alleles

HGVS	Amino-acid Change
NM_032801.5:c.410-14_410-13insCTT MANE Select	NP_116190.3:n.410-14_410-13insCTT
ENST00000299106.9:c.410-14_410-13insCTT MANE Select	ENSP00000299106.4:n.410-14_410-13insCTT
NM_001205329.1:c.257-14_257-13insCTT	NP_001192258.1:n.257-14_257-13insCTT
NM_001205329.2:c.257-14_257-13insCTT	NP_001192258.1:n.257-14_257-13insCTT
NM_032801.4:c.410-14_410-13insCTT	NP_116190.3:n.410-14_410-13insCTT
ENST00000299106.8:c.410-14_410-13insCTT	ENSP00000299106.4:n.410-14_410-13insCTT
ENST00000441717.3:c.257-14_257-13insCTT	ENSP00000395742.3:n.257-14_257-13insCTT
ENST00000524969.5:n.474-14_474-13insCTT
ENST00000531302.5:n.409-14_409-13insCTT
ENST00000532165.1:n.440-14_440-13insCTT
ENST00000532252.5:c.*400-14_*400-13insCTT	ENSP00000432455.1:n.*400-14_*400-13insCTT
ENST00000534549.5:c.230-14_230-13insCTT	ENSP00000433206.1:n.230-14_230-13insCTT