Canonical Allele Identifier: CA2620023802

Gene: PTPRQ

Linked Data

• gnomAD v4: 12-80484735-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80484735G>C , CM000674.2:g.80484735G>C	GRCh38
NC_000012.11:g.80878514G>C , CM000674.1:g.80878514G>C	GRCh37
NC_000012.10:g.79402645G>C	NCBI36
NG_034052.1:g.45390G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644991.3:c.1359+130G>C MANE Select	ENSP00000495607.1:n.1359+130G>C
ENST00000614701.4:c.1359+130G>C	ENSP00000482885.1:n.1359+130G>C
ENST00000616559.4:c.1485+130G>C	ENSP00000483259.1:n.1485+130G>C
NM_001145026.1:c.1359+130G>C	NP_001138498.1:n.1359+130G>C
XM_011538290.1:c.1359+130G>C	XP_011536592.1:n.1359+130G>C
XM_017019273.1:c.2025+130G>C	XP_016874762.1:n.2025+130G>C
XM_017019274.1:c.2025+130G>C	XP_016874763.1:n.2025+130G>C
XM_017019275.1:c.2025+130G>C	XP_016874764.1:n.2025+130G>C
XR_001748688.1:n.2162+130G>C
XR_001748689.1:n.2162+130G>C
NM_001145026.2:c.1359+130G>C MANE Select	NP_001138498.1:n.1359+130G>C