Canonical Allele Identifier: CA392886087

Gene: IGDCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.65384991G>A , CM000677.2:g.65384991G>A	GRCh38
NC_000015.9:g.65677329G>A , CM000677.1:g.65677329G>A	GRCh37
NC_000015.8:g.63464382G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_020962.3:c.3305C>T MANE Select	NP_066013.1:p.Thr1102Met
ENST00000352385.3:c.3305C>T MANE Select	ENSP00000319623.3:p.Thr1102Met
NM_020962.2:c.3305C>T	NP_066013.1:p.Thr1102Met
ENST00000352385.2:c.3305C>T	ENSP00000319623.3:p.Thr1102Met
ENST00000558048.5:n.437C>T
ENST00000559327.1:n.2574C>T
ENST00000561309.1:n.326C>T
XM_011521845.1:c.3344C>T	XP_011520147.1:p.Thr1115Met
XM_011521845.3:c.3344C>T	XP_011520147.1:p.Thr1115Met
XM_011521846.1:c.3308C>T	XP_011520148.1:p.Thr1103Met
XM_011521846.3:c.3308C>T	XP_011520148.1:p.Thr1103Met
XM_011521847.1:c.2522C>T	XP_011520149.1:p.Thr841Met
XM_011521847.2:c.2522C>T	XP_011520149.1:p.Thr841Met
XM_017022448.2:c.3347C>T	XP_016877937.1:p.Thr1116Met