Canonical Allele Identifier: CA2840347455

Gene: TMEM63A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.225852655dup , CM000663.2:g.225852655dup	GRCh38
NC_000001.10:g.226040356dup , CM000663.1:g.226040356dup	GRCh37
NC_000001.9:g.224106979dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366835.8:c.1903+11dup MANE Select	ENSP00000355800.3:n.1903+11dup
ENST00000366835.7:c.1903+11dup	ENSP00000355800.3:n.1903+11dup
NM_014698.2:c.1903+11dup	NP_055513.2:n.1903+11dup
XM_006711841.2:c.1372+11dup	XP_006711904.1:n.1372+11dup
XM_011544328.1:c.1903+11dup	XP_011542630.1:n.1903+11dup
XM_011544329.1:c.1903+11dup	XP_011542631.1:n.1903+11dup
XM_011544330.1:c.1903+11dup	XP_011542632.1:n.1903+11dup
XM_011544331.1:c.1816+11dup	XP_011542633.1:n.1816+11dup
XM_011544332.1:c.1462+11dup	XP_011542634.1:n.1462+11dup
XR_949163.1:n.2208+11dup
XM_006711841.4:c.1372+11dup	XP_006711904.1:n.1372+11dup
XM_011544328.3:c.1903+11dup	XP_011542630.1:n.1903+11dup
XM_011544329.3:c.1903+11dup	XP_011542631.1:n.1903+11dup
XM_011544330.3:c.1903+11dup	XP_011542632.1:n.1903+11dup
XM_011544331.3:c.1816+11dup	XP_011542633.1:n.1816+11dup
XM_011544332.3:c.1462+11dup	XP_011542634.1:n.1462+11dup
XR_001737552.2:n.1990+11dup
XR_949163.3:n.2187+11dup
NM_014698.3:c.1903+11dup MANE Select	NP_055513.2:n.1903+11dup