Canonical Allele Identifier: CA628367590

Gene: PTPRM

Linked Data

• dbSNP Id: rs1180961427
• gnomAD v2: 18-7755712-A-G
• gnomAD v3: 18-7755714-A-G
• gnomAD v4: 18-7755714-A-G
• MyVariant Identifiers: chr18:g.7755712A>G (hg19) ; chr18:g.7755714A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.7755714A>G , CM000680.2:g.7755714A>G	GRCh38
NC_000018.9:g.7755712A>G , CM000680.1:g.7755712A>G	GRCh37
NC_000018.8:g.7745712A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000580170.6:c.74-18435A>G MANE Select	ENSP00000463325.1:n.74-18435A>G
ENST00000332175.12:c.74-18435A>G	ENSP00000331418.8:n.74-18435A>G
ENST00000400053.8:c.-114+430A>G	ENSP00000382927.4:n.-114+430A>G
ENST00000580170.5:c.74-18435A>G	ENSP00000463325.1:n.74-18435A>G
NM_001105244.1:c.74-18435A>G	NP_001098714.1:n.74-18435A>G
NM_002845.3:c.74-18435A>G	NP_002836.3:n.74-18435A>G
XM_006722335.2:c.74-18435A>G	XP_006722398.1:n.74-18435A>G
XM_006722337.2:c.74-18435A>G	XP_006722400.1:n.74-18435A>G
XM_011525708.1:c.74-18435A>G	XP_011524010.1:n.74-18435A>G
XM_011525709.1:c.74-18435A>G	XP_011524011.1:n.74-18435A>G
XM_011525710.1:c.74-18435A>G	XP_011524012.1:n.74-18435A>G
XM_011525711.1:c.74-18435A>G	XP_011524013.1:n.74-18435A>G
XM_011525712.1:c.74-18435A>G	XP_011524014.1:n.74-18435A>G
XM_011525718.1:c.74-18435A>G	XP_011524020.1:n.74-18435A>G
XM_011525719.1:c.74-18435A>G	XP_011524021.1:n.74-18435A>G
XM_011525720.1:c.74-18435A>G	XP_011524022.1:n.74-18435A>G
XM_011525721.1:c.74-18435A>G	XP_011524023.1:n.74-18435A>G
XR_430046.2:n.572-18435A>G
XM_011525708.2:c.74-18435A>G	XP_011524010.1:n.74-18435A>G
XM_011525710.2:c.74-18435A>G	XP_011524012.1:n.74-18435A>G
XM_011525712.2:c.74-18435A>G	XP_011524014.1:n.74-18435A>G
XM_017025894.1:c.58+7219A>G	XP_016881383.1:n.58+7219A>G
XM_017025895.1:c.58+7219A>G	XP_016881384.1:n.58+7219A>G
XM_017025896.1:c.58+7219A>G	XP_016881385.1:n.58+7219A>G
XM_017025897.1:c.58+7219A>G	XP_016881386.1:n.58+7219A>G
XM_017025898.1:c.58+7219A>G	XP_016881387.1:n.58+7219A>G
XM_017025899.1:c.58+7219A>G	XP_016881388.1:n.58+7219A>G
XM_017025900.1:c.58+7219A>G	XP_016881389.1:n.58+7219A>G
XM_017025901.1:c.58+7219A>G	XP_016881390.1:n.58+7219A>G
XM_017025902.1:c.58+7219A>G	XP_016881391.1:n.58+7219A>G
XM_017025903.1:c.58+7219A>G	XP_016881392.1:n.58+7219A>G
XM_017025904.1:c.58+7219A>G	XP_016881393.1:n.58+7219A>G
XM_017025910.1:c.58+7219A>G	XP_016881399.1:n.58+7219A>G
XM_017025911.1:c.74-18435A>G	XP_016881400.1:n.74-18435A>G
XM_017025912.1:c.58+7219A>G	XP_016881401.1:n.58+7219A>G
XR_001753258.1:n.115+7219A>G
NM_001105244.2:c.74-18435A>G MANE Select	NP_001098714.1:n.74-18435A>G
NM_002845.4:c.74-18435A>G	NP_002836.3:n.74-18435A>G