Canonical Allele Identifier: CA2015276306
Gene: M6PR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8945311G= , CM000674.2:g.8945311G= GRCh38
NC_000012.11:g.9097907G= , CM000674.1:g.9097907G= GRCh37
NC_000012.10:g.8989174G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000000412.8:c.343+107C= MANE Select ENSP00000000412.3:n.343+107C=
ENST00000000412.7:c.343+107C= ENSP00000000412.3:n.343+107C=
ENST00000536844.5:c.343+107C= ENSP00000440488.2:n.343+107C=
ENST00000540837.1:n.574C=
ENST00000541507.5:c.343+107C= ENSP00000442100.1:n.343+107C=
ENST00000543258.1:c.179+107C=
ENST00000543704.5:c.66+992C= ENSP00000437595.1:n.66+992C=
ENST00000543834.1:n.62+107C=
ENST00000544245.1:c.-12+107C= ENSP00000439968.1:n.-12+107C=
NM_001207024.1:c.343+107C= NP_001193953.1:n.343+107C=
NM_002355.3:c.343+107C= NP_002346.1:n.343+107C=
XM_005253376.1:c.343+107C= XP_005253433.1:n.343+107C=
XM_011520672.1:c.343+107C= XP_011518974.1:n.343+107C=
XM_005253376.2:c.343+107C= XP_005253433.1:n.343+107C=
NM_002355.4:c.343+107C= MANE Select NP_002346.1:n.343+107C=
NM_001207024.2:c.343+107C= NP_001193953.1:n.343+107C=