Canonical Allele Identifier: CA2617524812

Gene: M6PR

Linked Data

• gnomAD v4: 12-8945338-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8945338G>T , CM000674.2:g.8945338G>T	GRCh38
NC_000012.11:g.9097934G>T , CM000674.1:g.9097934G>T	GRCh37
NC_000012.10:g.8989201G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000000412.8:c.343+80C>A MANE Select	ENSP00000000412.3:n.343+80C>A
ENST00000000412.7:c.343+80C>A	ENSP00000000412.3:n.343+80C>A
ENST00000536844.5:c.343+80C>A	ENSP00000440488.2:n.343+80C>A
ENST00000540837.1:n.547C>A
ENST00000541507.5:c.343+80C>A	ENSP00000442100.1:n.343+80C>A
ENST00000543258.1:c.179+80C>A
ENST00000543704.5:c.66+965C>A	ENSP00000437595.1:n.66+965C>A
ENST00000543834.1:n.62+80C>A
ENST00000544245.1:c.-12+80C>A	ENSP00000439968.1:n.-12+80C>A
NM_001207024.1:c.343+80C>A	NP_001193953.1:n.343+80C>A
NM_002355.3:c.343+80C>A	NP_002346.1:n.343+80C>A
XM_005253376.1:c.343+80C>A	XP_005253433.1:n.343+80C>A
XM_011520672.1:c.343+80C>A	XP_011518974.1:n.343+80C>A
XM_005253376.2:c.343+80C>A	XP_005253433.1:n.343+80C>A
NM_002355.4:c.343+80C>A MANE Select	NP_002346.1:n.343+80C>A
NM_001207024.2:c.343+80C>A	NP_001193953.1:n.343+80C>A