Canonical Allele Identifier: CA2614758776

Gene: TPCN2

Linked Data

• gnomAD v4: 11-69078931-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69078932del , CM000673.2:g.69078932del	GRCh38
NC_000011.9:g.68846400del , CM000673.1:g.68846400del	GRCh37
NC_000011.8:g.68602976del	NCBI36
NG_016153.1:g.35051del

Transcript Alleles

HGVS	Amino-acid change
ENST00000692585.1:c.308del	ENSP00000509200.1:p.Met103SerfsTer?
ENST00000294309.8:c.1451del MANE Select	ENSP00000294309.3:p.Met484SerfsTer?
ENST00000635811.1:c.1451del	ENSP00000490341.1:p.Met484SerfsTer?
ENST00000637084.1:c.308del	ENSP00000490615.1:p.Met103SerfsTer?
ENST00000637342.1:c.1451del	ENSP00000490171.1:p.Met484SerfsTer?
ENST00000637504.1:c.1451del	ENSP00000489759.1:p.Met484SerfsTer?
ENST00000294309.7:c.1451del	ENSP00000294309.3:p.Met484SerfsTer?
ENST00000442692.2:n.1044del
ENST00000535009.5:n.1260del
ENST00000542467.1:c.1451del	ENSP00000445551.1:p.Met484SerfsTer30
NM_139075.3:c.1451del	NP_620714.2:p.Met484SerfsTer?
XM_005273824.2:c.1448del	XP_005273881.1:p.Met483SerfsTer?
XM_005273826.2:c.1196del	XP_005273883.1:p.Met399SerfsTer?
XM_005273827.2:c.1451del	XP_005273884.1:p.Met484SerfsTer?
XM_005273828.2:c.1451del	XP_005273885.1:p.Met484SerfsTer?
XM_005273830.2:c.758del	XP_005273887.1:p.Met253SerfsTer?
XM_005273831.2:c.758del	XP_005273888.1:p.Met253SerfsTer?
XM_005273832.2:c.728del	XP_005273889.1:p.Met243SerfsTer?
XM_006718453.2:c.1451del	XP_006718516.1:p.Met484SerfsTer?
XM_006718454.2:c.1451del	XP_006718517.1:p.Met484SerfsTer?
XM_006718456.2:c.1451del	XP_006718519.1:p.Met484SerfsTer?
XM_011544802.1:c.1211del	XP_011543104.1:p.Met404SerfsTer?
XM_011544803.1:c.1451del	XP_011543105.1:p.Met484SerfsTer?
XM_011544804.1:c.1451del	XP_011543106.1:p.Met484SerfsTer?
XM_011544805.1:c.1451del	XP_011543107.1:p.Met484SerfsTer?
XM_011544806.1:c.1451del	XP_011543108.1:p.Met484SerfsTer?
XM_011544807.1:c.755del	XP_011543109.1:p.Met252SerfsTer?
XM_011544808.1:c.620del	XP_011543110.1:p.Met207SerfsTer?
XR_247191.1:n.1552del
XM_005273824.4:c.1448del	XP_005273881.1:p.Met483SerfsTer?
XM_005273826.4:c.1196del	XP_005273883.1:p.Met399SerfsTer?
XM_005273830.4:c.758del	XP_005273887.1:p.Met253SerfsTer?
XM_005273831.4:c.758del	XP_005273888.1:p.Met253SerfsTer?
XM_005273832.4:c.728del	XP_005273889.1:p.Met243SerfsTer?
XM_011544802.3:c.1211del	XP_011543104.1:p.Met404SerfsTer?
XM_011544807.3:c.755del	XP_011543109.1:p.Met252SerfsTer?
XM_011544808.3:c.620del	XP_011543110.1:p.Met207SerfsTer?
XM_017017328.2:c.1282del	XP_016872817.1:p.Cys428AlafsTer21
XM_017017329.2:c.1279del	XP_016872818.1:p.Cys427AlafsTer21
XM_017017330.2:c.728del	XP_016872819.1:p.Met243SerfsTer?
XM_017017331.2:c.728del	XP_016872820.1:p.Met243SerfsTer?
XM_017017332.2:c.542del	XP_016872821.1:p.Met181SerfsTer?
XM_017017333.2:c.559del	XP_016872822.1:p.Cys187AlafsTer21
XM_017017334.2:c.559del	XP_016872823.1:p.Cys187AlafsTer21
XM_017017335.2:c.559del	XP_016872824.1:p.Cys187AlafsTer21
XM_017017336.2:c.451del	XP_016872825.1:p.Cys151AlafsTer21
XM_024448392.1:c.1241del	XP_024304160.1:p.Met414SerfsTer?
XM_024448393.1:c.728del	XP_024304161.1:p.Met243SerfsTer?
XR_001747789.2:n.1383del
XR_001747790.2:n.1383del
XR_247191.3:n.1555del
NM_139075.4:c.1451del MANE Select	NP_620714.2:p.Met484SerfsTer?