Canonical Allele Identifier: CA2614758263

Gene: TPCN2

Linked Data

• gnomAD v4: 11-69078579-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69078581del , CM000673.2:g.69078581del	GRCh38
NC_000011.9:g.68846049del , CM000673.1:g.68846049del	GRCh37
NC_000011.8:g.68602625del	NCBI36
NG_016153.1:g.34700del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000692585.1:c.187del	ENSP00000509200.1:p.Ala63GlnfsTer?
ENST00000294309.8:c.1330del MANE Select	ENSP00000294309.3:p.Ala444GlnfsTer?
ENST00000635811.1:c.1330del	ENSP00000490341.1:p.Ala444GlnfsTer?
ENST00000637084.1:c.187del	ENSP00000490615.1:p.Ala63GlnfsTer?
ENST00000637342.1:c.1330del	ENSP00000490171.1:p.Ala444GlnfsTer?
ENST00000637504.1:c.1330del	ENSP00000489759.1:p.Ala444GlnfsTer?
ENST00000294309.7:c.1330del	ENSP00000294309.3:p.Ala444GlnfsTer?
ENST00000442692.2:n.923del
ENST00000535009.5:n.1139del
ENST00000542467.1:c.1330del	ENSP00000445551.1:p.Ala444GlnfsTer?
NM_139075.3:c.1330del	NP_620714.2:p.Ala444GlnfsTer?
XM_005273824.2:c.1327del	XP_005273881.1:p.Ala443GlnfsTer?
XM_005273826.2:c.1075del	XP_005273883.1:p.Ala359GlnfsTer?
XM_005273827.2:c.1330del	XP_005273884.1:p.Ala444GlnfsTer?
XM_005273828.2:c.1330del	XP_005273885.1:p.Ala444GlnfsTer?
XM_005273830.2:c.637del	XP_005273887.1:p.Ala213GlnfsTer?
XM_005273831.2:c.637del	XP_005273888.1:p.Ala213GlnfsTer?
XM_005273832.2:c.607del	XP_005273889.1:p.Ala203GlnfsTer?
XM_006718453.2:c.1330del	XP_006718516.1:p.Ala444GlnfsTer?
XM_006718454.2:c.1330del	XP_006718517.1:p.Ala444GlnfsTer?
XM_006718456.2:c.1330del	XP_006718519.1:p.Ala444GlnfsTer?
XM_011544802.1:c.1090del	XP_011543104.1:p.Ala364GlnfsTer?
XM_011544803.1:c.1330del	XP_011543105.1:p.Ala444GlnfsTer?
XM_011544804.1:c.1330del	XP_011543106.1:p.Ala444GlnfsTer?
XM_011544805.1:c.1330del	XP_011543107.1:p.Ala444GlnfsTer?
XM_011544806.1:c.1330del	XP_011543108.1:p.Ala444GlnfsTer?
XM_011544807.1:c.634del	XP_011543109.1:p.Ala212GlnfsTer?
XM_011544808.1:c.499del	XP_011543110.1:p.Ala167GlnfsTer?
XR_247191.1:n.1431del
XM_005273824.4:c.1327del	XP_005273881.1:p.Ala443GlnfsTer?
XM_005273826.4:c.1075del	XP_005273883.1:p.Ala359GlnfsTer?
XM_005273830.4:c.637del	XP_005273887.1:p.Ala213GlnfsTer?
XM_005273831.4:c.637del	XP_005273888.1:p.Ala213GlnfsTer?
XM_005273832.4:c.607del	XP_005273889.1:p.Ala203GlnfsTer?
XM_011544802.3:c.1090del	XP_011543104.1:p.Ala364GlnfsTer?
XM_011544807.3:c.634del	XP_011543109.1:p.Ala212GlnfsTer?
XM_011544808.3:c.499del	XP_011543110.1:p.Ala167GlnfsTer?
XM_017017328.2:c.1161del	XP_016872817.1:p.Trp387CysfsTer20
XM_017017329.2:c.1158del	XP_016872818.1:p.Trp386CysfsTer20
XM_017017330.2:c.607del	XP_016872819.1:p.Ala203GlnfsTer?
XM_017017331.2:c.607del	XP_016872820.1:p.Ala203GlnfsTer?
XM_017017332.2:c.421del	XP_016872821.1:p.Ala141GlnfsTer?
XM_017017333.2:c.438del	XP_016872822.1:p.Trp146CysfsTer20
XM_017017334.2:c.438del	XP_016872823.1:p.Trp146CysfsTer20
XM_017017335.2:c.438del	XP_016872824.1:p.Trp146CysfsTer20
XM_017017336.2:c.330del	XP_016872825.1:p.Trp110CysfsTer20
XM_024448392.1:c.1120del	XP_024304160.1:p.Ala374GlnfsTer?
XM_024448393.1:c.607del	XP_024304161.1:p.Ala203GlnfsTer?
XR_001747789.2:n.1262del
XR_001747790.2:n.1262del
XR_247191.3:n.1434del
NM_139075.4:c.1330del MANE Select	NP_620714.2:p.Ala444GlnfsTer?