Canonical Allele Identifier: CA1224646674
Gene: TMEM63A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.225852807_225852812delinsTCCACC , CM000663.2:g.225852807_225852812delinsTCCACC GRCh38
NC_000001.10:g.226040508_226040513delinsTCCACC , CM000663.1:g.226040508_226040513delinsTCCACC GRCh37
NC_000001.9:g.224107131_224107136delinsTCCACC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000366835.8:c.1798-43_1798-38delinsGGTGGA MANE Select ENSP00000355800.3:n.1798-43_1798-38delinsGGTGGA
ENST00000366835.7:c.1798-43_1798-38delinsGGTGGA ENSP00000355800.3:n.1798-43_1798-38delinsGGTGGA
NM_014698.2:c.1798-43_1798-38delinsGGTGGA NP_055513.2:n.1798-43_1798-38delinsGGTGGA
XM_006711841.2:c.1267-43_1267-38delinsGGTGGA XP_006711904.1:n.1267-43_1267-38delinsGGTGGA
XM_011544328.1:c.1798-43_1798-38delinsGGTGGA XP_011542630.1:n.1798-43_1798-38delinsGGTGGA
XM_011544329.1:c.1798-43_1798-38delinsGGTGGA XP_011542631.1:n.1798-43_1798-38delinsGGTGGA
XM_011544330.1:c.1798-43_1798-38delinsGGTGGA XP_011542632.1:n.1798-43_1798-38delinsGGTGGA
XM_011544331.1:c.1711-43_1711-38delinsGGTGGA XP_011542633.1:n.1711-43_1711-38delinsGGTGGA
XM_011544332.1:c.1357-43_1357-38delinsGGTGGA XP_011542634.1:n.1357-43_1357-38delinsGGTGGA
XR_949163.1:n.2103-43_2103-38delinsGGTGGA
XM_006711841.4:c.1267-43_1267-38delinsGGTGGA XP_006711904.1:n.1267-43_1267-38delinsGGTGGA
XM_011544328.3:c.1798-43_1798-38delinsGGTGGA XP_011542630.1:n.1798-43_1798-38delinsGGTGGA
XM_011544329.3:c.1798-43_1798-38delinsGGTGGA XP_011542631.1:n.1798-43_1798-38delinsGGTGGA
XM_011544330.3:c.1798-43_1798-38delinsGGTGGA XP_011542632.1:n.1798-43_1798-38delinsGGTGGA
XM_011544331.3:c.1711-43_1711-38delinsGGTGGA XP_011542633.1:n.1711-43_1711-38delinsGGTGGA
XM_011544332.3:c.1357-43_1357-38delinsGGTGGA XP_011542634.1:n.1357-43_1357-38delinsGGTGGA
XR_001737552.2:n.1885-43_1885-38delinsGGTGGA
XR_949163.3:n.2082-43_2082-38delinsGGTGGA
NM_014698.3:c.1798-43_1798-38delinsGGTGGA MANE Select NP_055513.2:n.1798-43_1798-38delinsGGTGGA