Canonical Allele Identifier: CA2839578450

Gene: TPCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69078811del , CM000673.2:g.69078811del	GRCh38
NC_000011.9:g.68846279del , CM000673.1:g.68846279del	GRCh37
NC_000011.8:g.68602855del	NCBI36
NG_016153.1:g.34930del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000692585.1:c.267+18del	ENSP00000509200.1:n.267+18del
ENST00000294309.8:c.1410+18del MANE Select	ENSP00000294309.3:n.1410+18del
ENST00000635811.1:c.1410+18del	ENSP00000490341.1:n.1410+18del
ENST00000637084.1:c.267+18del	ENSP00000490615.1:n.267+18del
ENST00000637342.1:c.1410+18del	ENSP00000490171.1:n.1410+18del
ENST00000637504.1:c.1410+18del	ENSP00000489759.1:n.1410+18del
ENST00000294309.7:c.1410+18del	ENSP00000294309.3:n.1410+18del
ENST00000442692.2:n.1003+18del
ENST00000535009.5:n.1219+18del
ENST00000542467.1:c.1410+18del	ENSP00000445551.1:n.1410+18del
NM_139075.3:c.1410+18del	NP_620714.2:n.1410+18del
XM_005273824.2:c.1407+18del	XP_005273881.1:n.1407+18del
XM_005273826.2:c.1155+18del	XP_005273883.1:n.1155+18del
XM_005273827.2:c.1410+18del	XP_005273884.1:n.1410+18del
XM_005273828.2:c.1410+18del	XP_005273885.1:n.1410+18del
XM_005273830.2:c.717+18del	XP_005273887.1:n.717+18del
XM_005273831.2:c.717+18del	XP_005273888.1:n.717+18del
XM_005273832.2:c.687+18del	XP_005273889.1:n.687+18del
XM_006718453.2:c.1410+18del	XP_006718516.1:n.1410+18del
XM_006718454.2:c.1410+18del	XP_006718517.1:n.1410+18del
XM_006718456.2:c.1410+18del	XP_006718519.1:n.1410+18del
XM_011544802.1:c.1170+18del	XP_011543104.1:n.1170+18del
XM_011544803.1:c.1410+18del	XP_011543105.1:n.1410+18del
XM_011544804.1:c.1410+18del	XP_011543106.1:n.1410+18del
XM_011544805.1:c.1410+18del	XP_011543107.1:n.1410+18del
XM_011544806.1:c.1410+18del	XP_011543108.1:n.1410+18del
XM_011544807.1:c.714+18del	XP_011543109.1:n.714+18del
XM_011544808.1:c.579+18del	XP_011543110.1:n.579+18del
XR_247191.1:n.1511+18del
XM_005273824.4:c.1407+18del	XP_005273881.1:n.1407+18del
XM_005273826.4:c.1155+18del	XP_005273883.1:n.1155+18del
XM_005273830.4:c.717+18del	XP_005273887.1:n.717+18del
XM_005273831.4:c.717+18del	XP_005273888.1:n.717+18del
XM_005273832.4:c.687+18del	XP_005273889.1:n.687+18del
XM_011544802.3:c.1170+18del	XP_011543104.1:n.1170+18del
XM_011544807.3:c.714+18del	XP_011543109.1:n.714+18del
XM_011544808.3:c.579+18del	XP_011543110.1:n.579+18del
XM_017017328.2:c.1241+18del	XP_016872817.1:n.1241+18del
XM_017017329.2:c.1238+18del	XP_016872818.1:n.1238+18del
XM_017017330.2:c.687+18del	XP_016872819.1:n.687+18del
XM_017017331.2:c.687+18del	XP_016872820.1:n.687+18del
XM_017017332.2:c.501+18del	XP_016872821.1:n.501+18del
XM_017017333.2:c.518+18del	XP_016872822.1:n.518+18del
XM_017017334.2:c.518+18del	XP_016872823.1:n.518+18del
XM_017017335.2:c.518+18del	XP_016872824.1:n.518+18del
XM_017017336.2:c.410+18del	XP_016872825.1:n.410+18del
XM_024448392.1:c.1200+18del	XP_024304160.1:n.1200+18del
XM_024448393.1:c.687+18del	XP_024304161.1:n.687+18del
XR_001747789.2:n.1342+18del
XR_001747790.2:n.1342+18del
XR_247191.3:n.1514+18del
NM_139075.4:c.1410+18del MANE Select	NP_620714.2:n.1410+18del