Canonical Allele Identifier: CA2574905832

Gene: TPCN2

Linked Data

• gnomAD v4: 11-69087985-GGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69087993_69087994del , CM000673.2:g.69087993_69087994del	GRCh38
NC_000011.9:g.68855461_68855462del , CM000673.1:g.68855461_68855462del	GRCh37
NC_000011.8:g.68612037_68612038del	NCBI36
NG_016153.1:g.44112_44113del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000692585.1:c.1156_1157del	ENSP00000509200.1:n.1156_1157del
ENST00000294309.8:c.*40_*41del MANE Select	ENSP00000294309.3:n.*40_*41del
ENST00000635811.1:c.*494_*495del	ENSP00000490341.1:n.*494_*495del
ENST00000637084.1:c.1156_1157del	ENSP00000490615.1:n.1156_1157del
ENST00000637342.1:c.2003+2063_2003+2064del	ENSP00000490171.1:n.2003+2063_2003+2064del
ENST00000637504.1:c.*33+2707_*33+2708del	ENSP00000489759.1:n.*33+2707_*33+2708del
ENST00000294309.7:c.*40_*41del	ENSP00000294309.3:n.*40_*41del
ENST00000442692.2:n.1765_1766del
ENST00000542467.1:c.*40_*41del	ENSP00000445551.1:n.*40_*41del
NM_139075.3:c.*40_*41del	NP_620714.2:n.*40_*41del
XM_005273824.2:c.*40_*41del	XP_005273881.1:n.*40_*41del
XM_005273826.2:c.*40_*41del	XP_005273883.1:n.*40_*41del
XM_005273830.2:c.*40_*41del	XP_005273887.1:n.*40_*41del
XM_005273831.2:c.*40_*41del	XP_005273888.1:n.*40_*41del
XM_005273832.2:c.*40_*41del	XP_005273889.1:n.*40_*41del
XM_006718453.2:c.1639+6494_1639+6495del	XP_006718516.1:n.1639+6494_1639+6495del
XM_006718454.2:c.1689+6494_1689+6495del	XP_006718517.1:n.1689+6494_1689+6495del
XM_011544802.1:c.*40_*41del	XP_011543104.1:n.*40_*41del
XM_011544807.1:c.*40_*41del	XP_011543109.1:n.*40_*41del
XM_011544808.1:c.*40_*41del	XP_011543110.1:n.*40_*41del
XM_005273824.4:c.*40_*41del	XP_005273881.1:n.*40_*41del
XM_005273826.4:c.*40_*41del	XP_005273883.1:n.*40_*41del
XM_005273830.4:c.*40_*41del	XP_005273887.1:n.*40_*41del
XM_005273831.4:c.*40_*41del	XP_005273888.1:n.*40_*41del
XM_005273832.4:c.*40_*41del	XP_005273889.1:n.*40_*41del
XM_011544802.3:c.*40_*41del	XP_011543104.1:n.*40_*41del
XM_011544807.3:c.*40_*41del	XP_011543109.1:n.*40_*41del
XM_011544808.3:c.*40_*41del	XP_011543110.1:n.*40_*41del
XM_017017328.2:c.*40_*41del	XP_016872817.1:n.*40_*41del
XM_017017329.2:c.*40_*41del	XP_016872818.1:n.*40_*41del
XM_017017330.2:c.*40_*41del	XP_016872819.1:n.*40_*41del
XM_017017331.2:c.*40_*41del	XP_016872820.1:n.*40_*41del
XM_017017332.2:c.*40_*41del	XP_016872821.1:n.*40_*41del
XM_017017333.2:c.*40_*41del	XP_016872822.1:n.*40_*41del
XM_017017334.2:c.*40_*41del	XP_016872823.1:n.*40_*41del
XM_017017335.2:c.*40_*41del	XP_016872824.1:n.*40_*41del
XM_017017336.2:c.*40_*41del	XP_016872825.1:n.*40_*41del
XM_024448392.1:c.*40_*41del	XP_024304160.1:n.*40_*41del
XM_024448393.1:c.*40_*41del	XP_024304161.1:n.*40_*41del
XR_001747789.2:n.2231_2232del
XR_247191.3:n.2353_2354del
NM_139075.4:c.*40_*41del MANE Select	NP_620714.2:n.*40_*41del