Canonical Allele Identifier: CA2614769399

Gene: TPCN2

Linked Data

• gnomAD v4: 11-69087910-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69087911dup , CM000673.2:g.69087911dup	GRCh38
NC_000011.9:g.68855379dup , CM000673.1:g.68855379dup	GRCh37
NC_000011.8:g.68611955dup	NCBI36
NG_016153.1:g.44030dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000692585.1:c.1074dup	ENSP00000509200.1:p.Glu359ArgfsTer?
ENST00000294309.8:c.2217dup MANE Select	ENSP00000294309.3:p.Glu740ArgfsTer?
ENST00000635811.1:c.*412dup	ENSP00000490341.1:n.*412dup
ENST00000637084.1:c.1074dup	ENSP00000490615.1:p.Glu359ArgfsTer?
ENST00000637342.1:c.2003+1981dup	ENSP00000490171.1:n.2003+1981dup
ENST00000637504.1:c.*33+2625dup	ENSP00000489759.1:n.*33+2625dup
ENST00000294309.7:c.2217dup	ENSP00000294309.3:p.Glu740ArgfsTer?
ENST00000442692.2:n.1683dup
ENST00000542467.1:c.1671dup	ENSP00000445551.1:p.Glu558ArgfsTer?
NM_139075.3:c.2217dup	NP_620714.2:p.Glu740ArgfsTer?
XM_005273824.2:c.2214dup	XP_005273881.1:p.Glu739ArgfsTer?
XM_005273826.2:c.1962dup	XP_005273883.1:p.Glu655ArgfsTer?
XM_005273830.2:c.1524dup	XP_005273887.1:p.Glu509ArgfsTer?
XM_005273831.2:c.1524dup	XP_005273888.1:p.Glu509ArgfsTer?
XM_005273832.2:c.1494dup	XP_005273889.1:p.Glu499ArgfsTer?
XM_006718453.2:c.1639+6412dup	XP_006718516.1:n.1639+6412dup
XM_006718454.2:c.1689+6412dup	XP_006718517.1:n.1689+6412dup
XM_011544802.1:c.1977dup	XP_011543104.1:p.Glu660ArgfsTer?
XM_011544807.1:c.1521dup	XP_011543109.1:p.Glu508ArgfsTer?
XM_011544808.1:c.1386dup	XP_011543110.1:p.Glu463ArgfsTer?
XR_247191.1:n.2268dup
XM_005273824.4:c.2214dup	XP_005273881.1:p.Glu739ArgfsTer?
XM_005273826.4:c.1962dup	XP_005273883.1:p.Glu655ArgfsTer?
XM_005273830.4:c.1524dup	XP_005273887.1:p.Glu509ArgfsTer?
XM_005273831.4:c.1524dup	XP_005273888.1:p.Glu509ArgfsTer?
XM_005273832.4:c.1494dup	XP_005273889.1:p.Glu499ArgfsTer?
XM_011544802.3:c.1977dup	XP_011543104.1:p.Glu660ArgfsTer?
XM_011544807.3:c.1521dup	XP_011543109.1:p.Glu508ArgfsTer?
XM_011544808.3:c.1386dup	XP_011543110.1:p.Glu463ArgfsTer?
XM_017017328.2:c.1998dup	XP_016872817.1:p.Glu667ArgfsTer?
XM_017017329.2:c.1995dup	XP_016872818.1:p.Glu666ArgfsTer?
XM_017017330.2:c.1494dup	XP_016872819.1:p.Glu499ArgfsTer?
XM_017017331.2:c.1494dup	XP_016872820.1:p.Glu499ArgfsTer?
XM_017017332.2:c.1308dup	XP_016872821.1:p.Glu437ArgfsTer?
XM_017017333.2:c.1275dup	XP_016872822.1:p.Glu426ArgfsTer?
XM_017017334.2:c.1275dup	XP_016872823.1:p.Glu426ArgfsTer?
XM_017017335.2:c.1275dup	XP_016872824.1:p.Glu426ArgfsTer?
XM_017017336.2:c.1167dup	XP_016872825.1:p.Glu390ArgfsTer?
XM_024448392.1:c.2007dup	XP_024304160.1:p.Glu670ArgfsTer?
XM_024448393.1:c.1494dup	XP_024304161.1:p.Glu499ArgfsTer?
XR_001747789.2:n.2149dup
XR_247191.3:n.2271dup
NM_139075.4:c.2217dup MANE Select	NP_620714.2:p.Glu740ArgfsTer?