Canonical Allele Identifier: CA645595443

Gene: TPCN2

Linked Data

• COSMIC: COSM298403

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69078922_69078924del , CM000673.2:g.69078922_69078924del	GRCh38
NC_000011.9:g.68846390_68846392del , CM000673.1:g.68846390_68846392del	GRCh37
NC_000011.8:g.68602966_68602968del	NCBI36
NG_016153.1:g.35041_35043del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000692585.1:c.298_300del	ENSP00000509200.1:p.Leu100del
ENST00000294309.8:c.1441_1443del MANE Select	ENSP00000294309.3:p.Leu481del
ENST00000635811.1:c.1441_1443del	ENSP00000490341.1:p.Leu481del
ENST00000637084.1:c.298_300del	ENSP00000490615.1:p.Leu100del
ENST00000637342.1:c.1441_1443del	ENSP00000490171.1:p.Leu481del
ENST00000637504.1:c.1441_1443del	ENSP00000489759.1:p.Leu481del
ENST00000294309.7:c.1441_1443del	ENSP00000294309.3:p.Leu481del
ENST00000442692.2:n.1034_1036del
ENST00000535009.5:n.1250_1252del
ENST00000542467.1:c.1441_1443del	ENSP00000445551.1:p.Leu481del
NM_139075.3:c.1441_1443del	NP_620714.2:p.Leu481del
XM_005273824.2:c.1438_1440del	XP_005273881.1:p.Leu480del
XM_005273826.2:c.1186_1188del	XP_005273883.1:p.Leu396del
XM_005273827.2:c.1441_1443del	XP_005273884.1:p.Leu481del
XM_005273828.2:c.1441_1443del	XP_005273885.1:p.Leu481del
XM_005273830.2:c.748_750del	XP_005273887.1:p.Leu250del
XM_005273831.2:c.748_750del	XP_005273888.1:p.Leu250del
XM_005273832.2:c.718_720del	XP_005273889.1:p.Leu240del
XM_006718453.2:c.1441_1443del	XP_006718516.1:p.Leu481del
XM_006718454.2:c.1441_1443del	XP_006718517.1:p.Leu481del
XM_006718456.2:c.1441_1443del	XP_006718519.1:p.Leu481del
XM_011544802.1:c.1201_1203del	XP_011543104.1:p.Leu401del
XM_011544803.1:c.1441_1443del	XP_011543105.1:p.Leu481del
XM_011544804.1:c.1441_1443del	XP_011543106.1:p.Leu481del
XM_011544805.1:c.1441_1443del	XP_011543107.1:p.Leu481del
XM_011544806.1:c.1441_1443del	XP_011543108.1:p.Leu481del
XM_011544807.1:c.745_747del	XP_011543109.1:p.Leu249del
XM_011544808.1:c.610_612del	XP_011543110.1:p.Leu204del
XR_247191.1:n.1542_1544del
XM_005273824.4:c.1438_1440del	XP_005273881.1:p.Leu480del
XM_005273826.4:c.1186_1188del	XP_005273883.1:p.Leu396del
XM_005273830.4:c.748_750del	XP_005273887.1:p.Leu250del
XM_005273831.4:c.748_750del	XP_005273888.1:p.Leu250del
XM_005273832.4:c.718_720del	XP_005273889.1:p.Leu240del
XM_011544802.3:c.1201_1203del	XP_011543104.1:p.Leu401del
XM_011544807.3:c.745_747del	XP_011543109.1:p.Leu249del
XM_011544808.3:c.610_612del	XP_011543110.1:p.Leu204del
XM_017017328.2:c.1272_1274del	XP_016872817.1:p.Cys425del
XM_017017329.2:c.1269_1271del	XP_016872818.1:p.Cys424del
XM_017017330.2:c.718_720del	XP_016872819.1:p.Leu240del
XM_017017331.2:c.718_720del	XP_016872820.1:p.Leu240del
XM_017017332.2:c.532_534del	XP_016872821.1:p.Leu178del
XM_017017333.2:c.549_551del	XP_016872822.1:p.Cys184del
XM_017017334.2:c.549_551del	XP_016872823.1:p.Cys184del
XM_017017335.2:c.549_551del	XP_016872824.1:p.Cys184del
XM_017017336.2:c.441_443del	XP_016872825.1:p.Cys148del
XM_024448392.1:c.1231_1233del	XP_024304160.1:p.Leu411del
XM_024448393.1:c.718_720del	XP_024304161.1:p.Leu240del
XR_001747789.2:n.1373_1375del
XR_001747790.2:n.1373_1375del
XR_247191.3:n.1545_1547del
NM_139075.4:c.1441_1443del MANE Select	NP_620714.2:p.Leu481del