Canonical Allele Identifier: CA2840347448

Gene: TMEM63A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.225852630dup , CM000663.2:g.225852630dup	GRCh38
NC_000001.10:g.226040331dup , CM000663.1:g.226040331dup	GRCh37
NC_000001.9:g.224106954dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366835.8:c.1903+36dup MANE Select	ENSP00000355800.3:n.1903+36dup
ENST00000366835.7:c.1903+36dup	ENSP00000355800.3:n.1903+36dup
NM_014698.2:c.1903+36dup	NP_055513.2:n.1903+36dup
XM_006711841.2:c.1372+36dup	XP_006711904.1:n.1372+36dup
XM_011544328.1:c.1903+36dup	XP_011542630.1:n.1903+36dup
XM_011544329.1:c.1903+36dup	XP_011542631.1:n.1903+36dup
XM_011544330.1:c.1903+36dup	XP_011542632.1:n.1903+36dup
XM_011544331.1:c.1816+36dup	XP_011542633.1:n.1816+36dup
XM_011544332.1:c.1462+36dup	XP_011542634.1:n.1462+36dup
XR_949163.1:n.2208+36dup
XM_006711841.4:c.1372+36dup	XP_006711904.1:n.1372+36dup
XM_011544328.3:c.1903+36dup	XP_011542630.1:n.1903+36dup
XM_011544329.3:c.1903+36dup	XP_011542631.1:n.1903+36dup
XM_011544330.3:c.1903+36dup	XP_011542632.1:n.1903+36dup
XM_011544331.3:c.1816+36dup	XP_011542633.1:n.1816+36dup
XM_011544332.3:c.1462+36dup	XP_011542634.1:n.1462+36dup
XR_001737552.2:n.1990+36dup
XR_949163.3:n.2187+36dup
NM_014698.3:c.1903+36dup MANE Select	NP_055513.2:n.1903+36dup