Canonical Allele Identifier: CA2614758663

Gene: TPCN2

Linked Data

• gnomAD v4: 11-69078875-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69078876del , CM000673.2:g.69078876del	GRCh38
NC_000011.9:g.68846344del , CM000673.1:g.68846344del	GRCh37
NC_000011.8:g.68602920del	NCBI36
NG_016153.1:g.34995del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000692585.1:c.268-16del	ENSP00000509200.1:n.268-16del
ENST00000294309.8:c.1411-16del MANE Select	ENSP00000294309.3:n.1411-16del
ENST00000635811.1:c.1411-16del	ENSP00000490341.1:n.1411-16del
ENST00000637084.1:c.268-16del	ENSP00000490615.1:n.268-16del
ENST00000637342.1:c.1411-16del	ENSP00000490171.1:n.1411-16del
ENST00000637504.1:c.1411-16del	ENSP00000489759.1:n.1411-16del
ENST00000294309.7:c.1411-16del	ENSP00000294309.3:n.1411-16del
ENST00000442692.2:n.1004-16del
ENST00000535009.5:n.1220-16del
ENST00000542467.1:c.1411-16del	ENSP00000445551.1:n.1411-16del
NM_139075.3:c.1411-16del	NP_620714.2:n.1411-16del
XM_005273824.2:c.1408-16del	XP_005273881.1:n.1408-16del
XM_005273826.2:c.1156-16del	XP_005273883.1:n.1156-16del
XM_005273827.2:c.1411-16del	XP_005273884.1:n.1411-16del
XM_005273828.2:c.1411-16del	XP_005273885.1:n.1411-16del
XM_005273830.2:c.718-16del	XP_005273887.1:n.718-16del
XM_005273831.2:c.718-16del	XP_005273888.1:n.718-16del
XM_005273832.2:c.688-16del	XP_005273889.1:n.688-16del
XM_006718453.2:c.1411-16del	XP_006718516.1:n.1411-16del
XM_006718454.2:c.1411-16del	XP_006718517.1:n.1411-16del
XM_006718456.2:c.1411-16del	XP_006718519.1:n.1411-16del
XM_011544802.1:c.1171-16del	XP_011543104.1:n.1171-16del
XM_011544803.1:c.1411-16del	XP_011543105.1:n.1411-16del
XM_011544804.1:c.1411-16del	XP_011543106.1:n.1411-16del
XM_011544805.1:c.1411-16del	XP_011543107.1:n.1411-16del
XM_011544806.1:c.1411-16del	XP_011543108.1:n.1411-16del
XM_011544807.1:c.715-16del	XP_011543109.1:n.715-16del
XM_011544808.1:c.580-16del	XP_011543110.1:n.580-16del
XR_247191.1:n.1512-16del
XM_005273824.4:c.1408-16del	XP_005273881.1:n.1408-16del
XM_005273826.4:c.1156-16del	XP_005273883.1:n.1156-16del
XM_005273830.4:c.718-16del	XP_005273887.1:n.718-16del
XM_005273831.4:c.718-16del	XP_005273888.1:n.718-16del
XM_005273832.4:c.688-16del	XP_005273889.1:n.688-16del
XM_011544802.3:c.1171-16del	XP_011543104.1:n.1171-16del
XM_011544807.3:c.715-16del	XP_011543109.1:n.715-16del
XM_011544808.3:c.580-16del	XP_011543110.1:n.580-16del
XM_017017328.2:c.1242-16del	XP_016872817.1:n.1242-16del
XM_017017329.2:c.1239-16del	XP_016872818.1:n.1239-16del
XM_017017330.2:c.688-16del	XP_016872819.1:n.688-16del
XM_017017331.2:c.688-16del	XP_016872820.1:n.688-16del
XM_017017332.2:c.502-16del	XP_016872821.1:n.502-16del
XM_017017333.2:c.519-16del	XP_016872822.1:n.519-16del
XM_017017334.2:c.519-16del	XP_016872823.1:n.519-16del
XM_017017335.2:c.519-16del	XP_016872824.1:n.519-16del
XM_017017336.2:c.411-16del	XP_016872825.1:n.411-16del
XM_024448392.1:c.1201-16del	XP_024304160.1:n.1201-16del
XM_024448393.1:c.688-16del	XP_024304161.1:n.688-16del
XR_001747789.2:n.1343-16del
XR_001747790.2:n.1343-16del
XR_247191.3:n.1515-16del
NM_139075.4:c.1411-16del MANE Select	NP_620714.2:n.1411-16del