Canonical Allele Identifier: CA2614758659

Gene: TPCN2

Linked Data

• gnomAD v4: 11-69078872-GCCTCTT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69078874_69078879del , CM000673.2:g.69078874_69078879del	GRCh38
NC_000011.9:g.68846342_68846347del , CM000673.1:g.68846342_68846347del	GRCh37
NC_000011.8:g.68602918_68602923del	NCBI36
NG_016153.1:g.34993_34998del

Transcript Alleles

HGVS	Amino-acid change
ENST00000692585.1:c.268-18_268-13del	ENSP00000509200.1:n.268-18_268-13del
ENST00000294309.8:c.1411-18_1411-13del MANE Select	ENSP00000294309.3:n.1411-18_1411-13del
ENST00000635811.1:c.1411-18_1411-13del	ENSP00000490341.1:n.1411-18_1411-13del
ENST00000637084.1:c.268-18_268-13del	ENSP00000490615.1:n.268-18_268-13del
ENST00000637342.1:c.1411-18_1411-13del	ENSP00000490171.1:n.1411-18_1411-13del
ENST00000637504.1:c.1411-18_1411-13del	ENSP00000489759.1:n.1411-18_1411-13del
ENST00000294309.7:c.1411-18_1411-13del	ENSP00000294309.3:n.1411-18_1411-13del
ENST00000442692.2:n.1004-18_1004-13del
ENST00000535009.5:n.1220-18_1220-13del
ENST00000542467.1:c.1411-18_1411-13del	ENSP00000445551.1:n.1411-18_1411-13del
NM_139075.3:c.1411-18_1411-13del	NP_620714.2:n.1411-18_1411-13del
XM_005273824.2:c.1408-18_1408-13del	XP_005273881.1:n.1408-18_1408-13del
XM_005273826.2:c.1156-18_1156-13del	XP_005273883.1:n.1156-18_1156-13del
XM_005273827.2:c.1411-18_1411-13del	XP_005273884.1:n.1411-18_1411-13del
XM_005273828.2:c.1411-18_1411-13del	XP_005273885.1:n.1411-18_1411-13del
XM_005273830.2:c.718-18_718-13del	XP_005273887.1:n.718-18_718-13del
XM_005273831.2:c.718-18_718-13del	XP_005273888.1:n.718-18_718-13del
XM_005273832.2:c.688-18_688-13del	XP_005273889.1:n.688-18_688-13del
XM_006718453.2:c.1411-18_1411-13del	XP_006718516.1:n.1411-18_1411-13del
XM_006718454.2:c.1411-18_1411-13del	XP_006718517.1:n.1411-18_1411-13del
XM_006718456.2:c.1411-18_1411-13del	XP_006718519.1:n.1411-18_1411-13del
XM_011544802.1:c.1171-18_1171-13del	XP_011543104.1:n.1171-18_1171-13del
XM_011544803.1:c.1411-18_1411-13del	XP_011543105.1:n.1411-18_1411-13del
XM_011544804.1:c.1411-18_1411-13del	XP_011543106.1:n.1411-18_1411-13del
XM_011544805.1:c.1411-18_1411-13del	XP_011543107.1:n.1411-18_1411-13del
XM_011544806.1:c.1411-18_1411-13del	XP_011543108.1:n.1411-18_1411-13del
XM_011544807.1:c.715-18_715-13del	XP_011543109.1:n.715-18_715-13del
XM_011544808.1:c.580-18_580-13del	XP_011543110.1:n.580-18_580-13del
XR_247191.1:n.1512-18_1512-13del
XM_005273824.4:c.1408-18_1408-13del	XP_005273881.1:n.1408-18_1408-13del
XM_005273826.4:c.1156-18_1156-13del	XP_005273883.1:n.1156-18_1156-13del
XM_005273830.4:c.718-18_718-13del	XP_005273887.1:n.718-18_718-13del
XM_005273831.4:c.718-18_718-13del	XP_005273888.1:n.718-18_718-13del
XM_005273832.4:c.688-18_688-13del	XP_005273889.1:n.688-18_688-13del
XM_011544802.3:c.1171-18_1171-13del	XP_011543104.1:n.1171-18_1171-13del
XM_011544807.3:c.715-18_715-13del	XP_011543109.1:n.715-18_715-13del
XM_011544808.3:c.580-18_580-13del	XP_011543110.1:n.580-18_580-13del
XM_017017328.2:c.1242-18_1242-13del	XP_016872817.1:n.1242-18_1242-13del
XM_017017329.2:c.1239-18_1239-13del	XP_016872818.1:n.1239-18_1239-13del
XM_017017330.2:c.688-18_688-13del	XP_016872819.1:n.688-18_688-13del
XM_017017331.2:c.688-18_688-13del	XP_016872820.1:n.688-18_688-13del
XM_017017332.2:c.502-18_502-13del	XP_016872821.1:n.502-18_502-13del
XM_017017333.2:c.519-18_519-13del	XP_016872822.1:n.519-18_519-13del
XM_017017334.2:c.519-18_519-13del	XP_016872823.1:n.519-18_519-13del
XM_017017335.2:c.519-18_519-13del	XP_016872824.1:n.519-18_519-13del
XM_017017336.2:c.411-18_411-13del	XP_016872825.1:n.411-18_411-13del
XM_024448392.1:c.1201-18_1201-13del	XP_024304160.1:n.1201-18_1201-13del
XM_024448393.1:c.688-18_688-13del	XP_024304161.1:n.688-18_688-13del
XR_001747789.2:n.1343-18_1343-13del
XR_001747790.2:n.1343-18_1343-13del
XR_247191.3:n.1515-18_1515-13del
NM_139075.4:c.1411-18_1411-13del MANE Select	NP_620714.2:n.1411-18_1411-13del