Canonical Allele Identifier: CA345012541

Gene: TMEM63A

Linked Data

• MyVariant Identifiers: chr1:g.226040405G>C (hg19) ; chr1:g.225852704G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.225852704G>C , CM000663.2:g.225852704G>C	GRCh38
NC_000001.10:g.226040405G>C , CM000663.1:g.226040405G>C	GRCh37
NC_000001.9:g.224107028G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000366835.8:c.1863C>G MANE Select	ENSP00000355800.3:p.Ile621Met
ENST00000366835.7:c.1863C>G	ENSP00000355800.3:p.Ile621Met
NM_014698.2:c.1863C>G	NP_055513.2:p.Ile621Met
XM_006711841.2:c.1332C>G	XP_006711904.1:p.Ile444Met
XM_011544328.1:c.1863C>G	XP_011542630.1:p.Ile621Met
XM_011544329.1:c.1863C>G	XP_011542631.1:p.Ile621Met
XM_011544330.1:c.1863C>G	XP_011542632.1:p.Ile621Met
XM_011544331.1:c.1776C>G	XP_011542633.1:p.Ile592Met
XM_011544332.1:c.1422C>G	XP_011542634.1:p.Ile474Met
XR_949163.1:n.2168C>G
XM_006711841.4:c.1332C>G	XP_006711904.1:p.Ile444Met
XM_011544328.3:c.1863C>G	XP_011542630.1:p.Ile621Met
XM_011544329.3:c.1863C>G	XP_011542631.1:p.Ile621Met
XM_011544330.3:c.1863C>G	XP_011542632.1:p.Ile621Met
XM_011544331.3:c.1776C>G	XP_011542633.1:p.Ile592Met
XM_011544332.3:c.1422C>G	XP_011542634.1:p.Ile474Met
XR_001737552.2:n.1950C>G
XR_949163.3:n.2147C>G
NM_014698.3:c.1863C>G MANE Select	NP_055513.2:p.Ile621Met