Canonical Allele Identifier: CA1165668569

Gene: PTPRF

Linked Data

• dbSNP Id: rs12076635

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43560985G>T , CM000663.2:g.43560985G>T	GRCh38
NC_000001.10:g.44026656G>T , CM000663.1:g.44026656G>T	GRCh37
NC_000001.9:g.43799243G>T	NCBI36
NG_047072.1:g.43748G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000359947.9:c.379+7044G>T MANE Select	ENSP00000353030.4:n.379+7044G>T
ENST00000359947.8:c.379+7044G>T	ENSP00000353030.4:n.379+7044G>T
ENST00000372405.1:n.504+7044G>T
ENST00000436724.5:n.692+7044G>T
ENST00000437607.1:c.379+7044G>T	ENSP00000413306.1:n.379+7044G>T
ENST00000438120.5:c.379+7044G>T	ENSP00000398822.1:n.379+7044G>T
ENST00000617451.4:c.379+7044G>T	ENSP00000483557.1:n.379+7044G>T
NM_002840.3:c.379+7044G>T	NP_002831.2:n.379+7044G>T
NM_130440.2:c.379+7044G>T	NP_569707.2:n.379+7044G>T
XM_005271079.2:c.379+7044G>T	XP_005271136.1:n.379+7044G>T
XM_005271080.2:c.379+7044G>T	XP_005271137.1:n.379+7044G>T
XM_005271081.2:c.379+7044G>T	XP_005271138.1:n.379+7044G>T
XM_005271082.2:c.379+7044G>T	XP_005271139.1:n.379+7044G>T
XM_006710795.2:c.379+7044G>T	XP_006710858.1:n.379+7044G>T
XM_006710796.2:c.379+7044G>T	XP_006710859.1:n.379+7044G>T
XM_006710797.2:c.379+7044G>T	XP_006710860.1:n.379+7044G>T
XM_006710798.2:c.379+7044G>T	XP_006710861.1:n.379+7044G>T
XM_006710799.2:c.379+7044G>T	XP_006710862.1:n.379+7044G>T
XM_006710800.2:c.379+7044G>T	XP_006710863.1:n.379+7044G>T
XM_006710801.2:c.379+7044G>T	XP_006710864.1:n.379+7044G>T
XM_011541871.1:c.379+7044G>T	XP_011540173.1:n.379+7044G>T
XM_011541872.1:c.379+7044G>T	XP_011540174.1:n.379+7044G>T
XM_011541873.1:c.379+7044G>T	XP_011540175.1:n.379+7044G>T
NM_001329137.1:c.379+7044G>T	NP_001316066.1:n.379+7044G>T
NM_001329138.1:c.379+7044G>T	NP_001316067.1:n.379+7044G>T
NM_001329139.1:c.379+7044G>T	NP_001316068.1:n.379+7044G>T
NM_001329140.1:c.379+7044G>T	NP_001316069.1:n.379+7044G>T
NM_002840.4:c.379+7044G>T	NP_002831.2:n.379+7044G>T
NM_130440.3:c.379+7044G>T	NP_569707.2:n.379+7044G>T
XM_005271079.3:c.379+7044G>T	XP_005271136.1:n.379+7044G>T
XM_005271080.3:c.379+7044G>T	XP_005271137.1:n.379+7044G>T
XM_005271081.3:c.379+7044G>T	XP_005271138.1:n.379+7044G>T
XM_005271082.3:c.379+7044G>T	XP_005271139.1:n.379+7044G>T
XM_006710795.3:c.379+7044G>T	XP_006710858.1:n.379+7044G>T
XM_006710796.3:c.379+7044G>T	XP_006710859.1:n.379+7044G>T
XM_006710797.3:c.379+7044G>T	XP_006710860.1:n.379+7044G>T
XM_006710798.3:c.379+7044G>T	XP_006710861.1:n.379+7044G>T
XM_006710799.3:c.379+7044G>T	XP_006710862.1:n.379+7044G>T
XM_006710800.3:c.379+7044G>T	XP_006710863.1:n.379+7044G>T
XM_006710801.3:c.379+7044G>T	XP_006710864.1:n.379+7044G>T
XM_011541871.3:c.379+7044G>T	XP_011540173.1:n.379+7044G>T
XM_011541872.3:c.379+7044G>T	XP_011540174.1:n.379+7044G>T
XM_011541873.2:c.379+7044G>T	XP_011540175.1:n.379+7044G>T
XM_017001942.2:c.349+7044G>T	XP_016857431.1:n.349+7044G>T
XM_017001943.1:c.379+7044G>T	XP_016857432.1:n.379+7044G>T
XM_017001944.1:c.379+7044G>T	XP_016857433.1:n.379+7044G>T
XM_017001945.1:c.379+7044G>T	XP_016857434.1:n.379+7044G>T
XM_017001946.1:c.379+7044G>T	XP_016857435.1:n.379+7044G>T
XM_017001949.1:c.379+7044G>T	XP_016857438.1:n.379+7044G>T
NM_002840.5:c.379+7044G>T MANE Select	NP_002831.2:n.379+7044G>T
NM_001329137.2:c.379+7044G>T	NP_001316066.1:n.379+7044G>T
NM_001329138.2:c.379+7044G>T	NP_001316067.1:n.379+7044G>T
NM_001329139.2:c.379+7044G>T	NP_001316068.1:n.379+7044G>T
NM_001329140.2:c.379+7044G>T	NP_001316069.1:n.379+7044G>T
NM_130440.4:c.379+7044G>T	NP_569707.2:n.379+7044G>T