Canonical Allele Identifier: CA1880623974

Gene: PTPA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.129148365G= , CM000671.2:g.129148365G=	GRCh38
NC_000009.11:g.131910644G= , CM000671.1:g.131910644G=	GRCh37
NC_000009.10:g.130950465G=	NCBI36
NG_029370.1:g.42417G=

Transcript Alleles

HGVS	Amino-acid Change
NM_178000.3:c.*901G= MANE Select	NP_821067.1:n.*901G=
ENST00000393370.7:c.*901G= MANE Select	ENSP00000377036.2:n.*901G=
NM_001193397.1:c.*901G=	NP_001180326.1:n.*901G=
NM_001193397.2:c.*901G=	NP_001180326.1:n.*901G=
NM_001271832.1:c.*901G=	NP_001258761.1:n.*901G=
NM_001271832.2:c.*901G=	NP_001258761.1:n.*901G=
NM_021131.4:c.*901G=	NP_066954.2:n.*901G=
NM_021131.5:c.*901G=	NP_066954.2:n.*901G=
NM_178000.2:c.*901G=	NP_821067.1:n.*901G=
NM_178001.2:c.*901G=	NP_821068.1:n.*901G=
NM_178001.3:c.*901G=	NP_821068.1:n.*901G=
NM_178003.2:c.*901G=	NP_821070.1:n.*901G=
NM_178003.3:c.*901G=	NP_821070.1:n.*901G=
ENST00000337738.5:c.*901G=	ENSP00000337448.1:n.*901G=
ENST00000337738.6:c.*901G=	ENSP00000337448.1:n.*901G=
ENST00000347048.8:c.*901G=	ENSP00000337412.4:n.*901G=
ENST00000348141.9:c.*901G=	ENSP00000335200.6:n.*901G=
ENST00000355007.7:c.*901G=	ENSP00000347109.3:n.*901G=
ENST00000357197.8:c.*901G=	ENSP00000349726.4:n.*901G=
ENST00000358994.8:c.*901G=	ENSP00000351885.4:n.*901G=
ENST00000358994.9:c.*901G=	ENSP00000351885.5:n.*901G=
ENST00000393370.6:c.*901G=	ENSP00000377036.2:n.*901G=
ENST00000452489.6:c.*901G=	ENSP00000394338.3:n.*901G=
ENST00000674559.1:c.108+5813G=	ENSP00000502494.1:n.108+5813G=
ENST00000674648.1:c.108+5813G=	ENSP00000502744.1:n.108+5813G=
XM_011518838.1:c.*901G=	XP_011517140.1:n.*901G=
XM_011518838.2:c.*901G=	XP_011517140.1:n.*901G=