Canonical Allele Identifier: CA2521194735

Gene: PTPRD

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.9924566T>A , CM000671.2:g.9924566T>A	GRCh38
NC_000009.11:g.9924566T>A , CM000671.1:g.9924566T>A	GRCh37
NC_000009.10:g.9914566T>A	NCBI36
NG_033963.1:g.693158A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381196.9:c.-368+13941A>T MANE Select	ENSP00000370593.3:n.-368+13941A>T
ENST00000381196.8:c.-368+13941A>T	ENSP00000370593.3:n.-368+13941A>T
ENST00000463477.5:c.-440+13941A>T	ENSP00000417661.1:n.-440+13941A>T
NM_002839.3:c.-368+13941A>T	NP_002830.1:n.-368+13941A>T
XM_011517980.1:c.-329+13941A>T	XP_011516282.1:n.-329+13941A>T
XM_011517992.1:c.-368+13941A>T	XP_011516294.1:n.-368+13941A>T
XM_006716817.4:c.-368+13941A>T	XP_006716880.1:n.-368+13941A>T
XM_006716823.3:c.-368+13941A>T	XP_006716886.1:n.-368+13941A>T
XM_006716825.4:c.-368+13941A>T	XP_006716888.1:n.-368+13941A>T
XM_006716827.4:c.-368+13941A>T	XP_006716890.1:n.-368+13941A>T
XM_006716832.4:c.-368+13941A>T	XP_006716895.1:n.-368+13941A>T
XM_006716833.4:c.-368+13941A>T	XP_006716896.1:n.-368+13941A>T
XM_006716834.4:c.-368+13941A>T	XP_006716897.1:n.-368+13941A>T
XM_006716835.4:c.-368+13941A>T	XP_006716898.1:n.-368+13941A>T
XM_006716837.4:c.-368+13941A>T	XP_006716900.1:n.-368+13941A>T
XM_011517992.3:c.-368+13941A>T	XP_011516294.1:n.-368+13941A>T
XM_017014958.2:c.-368+13941A>T	XP_016870447.1:n.-368+13941A>T
XM_017014959.2:c.-440+13941A>T	XP_016870448.1:n.-440+13941A>T
XM_017014960.2:c.-329+13941A>T	XP_016870449.1:n.-329+13941A>T
XM_017014961.2:c.-368+13941A>T	XP_016870450.1:n.-368+13941A>T
XM_017014963.2:c.-368+13941A>T	XP_016870452.1:n.-368+13941A>T
XM_017014964.2:c.-368+13941A>T	XP_016870453.1:n.-368+13941A>T
XM_017014965.2:c.-368+13941A>T	XP_016870454.1:n.-368+13941A>T
XM_017014966.2:c.-368+13941A>T	XP_016870455.1:n.-368+13941A>T
XM_017014967.2:c.-368+13941A>T	XP_016870456.1:n.-368+13941A>T
XM_017014968.2:c.-368+13941A>T	XP_016870457.1:n.-368+13941A>T
XM_017014969.2:c.-368+13941A>T	XP_016870458.1:n.-368+13941A>T
XM_017014970.2:c.-368+13941A>T	XP_016870459.1:n.-368+13941A>T
XM_017014971.2:c.-368+13941A>T	XP_016870460.1:n.-368+13941A>T
XM_017014972.2:c.-368+13941A>T	XP_016870461.1:n.-368+13941A>T
XM_017014973.2:c.-368+13941A>T	XP_016870462.1:n.-368+13941A>T
XM_017014974.2:c.-368+13941A>T	XP_016870463.1:n.-368+13941A>T
XM_017014975.2:c.-368+13941A>T	XP_016870464.1:n.-368+13941A>T
XM_017014976.2:c.-368+13941A>T	XP_016870465.1:n.-368+13941A>T
XM_017014977.2:c.-368+13941A>T	XP_016870466.1:n.-368+13941A>T
XM_017014978.2:c.-368+13941A>T	XP_016870467.1:n.-368+13941A>T
XM_017014979.2:c.-368+13941A>T	XP_016870468.1:n.-368+13941A>T
XM_017014980.2:c.-368+13941A>T	XP_016870469.1:n.-368+13941A>T
XM_017014981.2:c.-368+13941A>T	XP_016870470.1:n.-368+13941A>T
XM_017014982.2:c.-368+13941A>T	XP_016870471.1:n.-368+13941A>T
XM_017014983.2:c.-368+13941A>T	XP_016870472.1:n.-368+13941A>T
XM_017014984.2:c.-368+13941A>T	XP_016870473.1:n.-368+13941A>T
XM_017014985.2:c.-368+13941A>T	XP_016870474.1:n.-368+13941A>T
XM_017014986.2:c.-368+13941A>T	XP_016870475.1:n.-368+13941A>T
XM_017014987.2:c.-368+13941A>T	XP_016870476.1:n.-368+13941A>T
XM_017014988.2:c.-368+13941A>T	XP_016870477.1:n.-368+13941A>T
XM_017014989.2:c.-368+13941A>T	XP_016870478.1:n.-368+13941A>T
XM_017014990.2:c.-368+13941A>T	XP_016870479.1:n.-368+13941A>T
XM_017014991.2:c.-368+13941A>T	XP_016870480.1:n.-368+13941A>T
XM_017014992.2:c.-368+13941A>T	XP_016870481.1:n.-368+13941A>T
XM_017014993.2:c.-368+13941A>T	XP_016870482.1:n.-368+13941A>T
XM_017014994.2:c.-368+13941A>T	XP_016870483.1:n.-368+13941A>T
XM_017014995.2:c.-368+13941A>T	XP_016870484.1:n.-368+13941A>T
XM_024447625.1:c.-368+13941A>T	XP_024303393.1:n.-368+13941A>T
XM_024447627.1:c.-5819+13941A>T	XP_024303395.1:n.-5819+13941A>T
NM_002839.4:c.-368+13941A>T MANE Select	NP_002830.1:n.-368+13941A>T