Canonical Allele Identifier: CA2792562465

Gene: TPCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69078601_69078602del , CM000673.2:g.69078601_69078602del	GRCh38
NC_000011.9:g.68846069_68846070del , CM000673.1:g.68846069_68846070del	GRCh37
NC_000011.8:g.68602645_68602646del	NCBI36
NG_016153.1:g.34720_34721del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000692585.1:c.207_207+1del
ENST00000294309.8:c.1350_1350+1del
ENST00000635811.1:c.1350_1350+1del
ENST00000637084.1:c.207_207+1del
ENST00000637342.1:c.1350_1350+1del
ENST00000637504.1:c.1350_1350+1del
ENST00000294309.7:c.1350_1350+1del
ENST00000442692.2:n.943_943+1del
ENST00000535009.5:n.1159_1159+1del
ENST00000542467.1:c.1350_1350+1del
NM_139075.3:c.1350_1350+1del
XM_005273824.2:c.1347_1347+1del
XM_005273826.2:c.1095_1095+1del
XM_005273827.2:c.1350_1350+1del
XM_005273828.2:c.1350_1350+1del
XM_005273830.2:c.657_657+1del
XM_005273831.2:c.657_657+1del
XM_005273832.2:c.627_627+1del
XM_006718453.2:c.1350_1350+1del
XM_006718454.2:c.1350_1350+1del
XM_006718456.2:c.1350_1350+1del
XM_011544802.1:c.1110_1110+1del
XM_011544803.1:c.1350_1350+1del
XM_011544804.1:c.1350_1350+1del
XM_011544805.1:c.1350_1350+1del
XM_011544806.1:c.1350_1350+1del
XM_011544807.1:c.654_654+1del
XM_011544808.1:c.519_519+1del
XR_247191.1:n.1451_1451+1del
XM_005273824.4:c.1347_1347+1del
XM_005273826.4:c.1095_1095+1del
XM_005273830.4:c.657_657+1del
XM_005273831.4:c.657_657+1del
XM_005273832.4:c.627_627+1del
XM_011544802.3:c.1110_1110+1del
XM_011544807.3:c.654_654+1del
XM_011544808.3:c.519_519+1del
XM_017017328.2:c.1181_1181+1del
XM_017017329.2:c.1178_1178+1del
XM_017017330.2:c.627_627+1del
XM_017017331.2:c.627_627+1del
XM_017017332.2:c.441_441+1del
XM_017017333.2:c.458_458+1del
XM_017017334.2:c.458_458+1del
XM_017017335.2:c.458_458+1del
XM_017017336.2:c.350_350+1del
XM_024448392.1:c.1140_1140+1del
XM_024448393.1:c.627_627+1del
XR_001747789.2:n.1282_1282+1del
XR_001747790.2:n.1282_1282+1del
XR_247191.3:n.1454_1454+1del
NM_139075.4:c.1350_1350+1del