Canonical Allele Identifier: CA385875642
Gene: PTPRQ HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.80460663A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.80460663A>G , CM000674.2:g.80460663A>G GRCh38
NC_000012.11:g.80849514T>C , CM000674.1:g.80849514T>C GRCh37
NC_000012.10:g.79373645T>C NCBI36
NG_034052.1:g.21318A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000644991.3:c.671A>G MANE Select ENSP00000495607.1:p.Glu224Gly
ENST00000614701.4:c.671A>G ENSP00000482885.1:p.Glu224Gly
ENST00000616559.4:c.797A>G ENSP00000483259.1:p.Glu266Gly
NM_001145026.1:c.671A>G NP_001138498.1:p.Glu224Gly
XM_011538290.1:c.671A>G XP_011536592.1:p.Glu224Gly
XM_017019273.1:c.1337A>G XP_016874762.1:p.Glu446Gly
XM_017019274.1:c.1337A>G XP_016874763.1:p.Glu446Gly
XM_017019275.1:c.1337A>G XP_016874764.1:p.Glu446Gly
XR_001748688.1:n.1474A>G
XR_001748689.1:n.1474A>G
NM_001145026.2:c.671A>G MANE Select NP_001138498.1:p.Glu224Gly