Canonical Allele Identifier: CA6155217

Gene: TPCN2

Linked Data

• dbSNP Id: rs766315718
• ExAC: 11:68846099 CG / C
• gnomAD v2: 11-68846099-CG-C
• gnomAD v3: 11-69078631-CG-C
• gnomAD v4: 11-69078631-CG-C
• MyVariant Identifiers: chr11:g.68846100del (hg19) ; chr11:g.69078632del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69078633del , CM000673.2:g.69078633del	GRCh38
NC_000011.9:g.68846101del , CM000673.1:g.68846101del	GRCh37
NC_000011.8:g.68602677del	NCBI36
NG_016153.1:g.34752del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000692585.1:c.207+32del	ENSP00000509200.1:n.207+32del
ENST00000294309.8:c.1350+32del MANE Select	ENSP00000294309.3:n.1350+32del
ENST00000635811.1:c.1350+32del	ENSP00000490341.1:n.1350+32del
ENST00000637084.1:c.207+32del	ENSP00000490615.1:n.207+32del
ENST00000637342.1:c.1350+32del	ENSP00000490171.1:n.1350+32del
ENST00000637504.1:c.1350+32del	ENSP00000489759.1:n.1350+32del
ENST00000294309.7:c.1350+32del	ENSP00000294309.3:n.1350+32del
ENST00000442692.2:n.943+32del
ENST00000535009.5:n.1159+32del
ENST00000542467.1:c.1350+32del	ENSP00000445551.1:n.1350+32del
NM_139075.3:c.1350+32del	NP_620714.2:n.1350+32del
XM_005273824.2:c.1347+32del	XP_005273881.1:n.1347+32del
XM_005273826.2:c.1095+32del	XP_005273883.1:n.1095+32del
XM_005273827.2:c.1350+32del	XP_005273884.1:n.1350+32del
XM_005273828.2:c.1350+32del	XP_005273885.1:n.1350+32del
XM_005273830.2:c.657+32del	XP_005273887.1:n.657+32del
XM_005273831.2:c.657+32del	XP_005273888.1:n.657+32del
XM_005273832.2:c.627+32del	XP_005273889.1:n.627+32del
XM_006718453.2:c.1350+32del	XP_006718516.1:n.1350+32del
XM_006718454.2:c.1350+32del	XP_006718517.1:n.1350+32del
XM_006718456.2:c.1350+32del	XP_006718519.1:n.1350+32del
XM_011544802.1:c.1110+32del	XP_011543104.1:n.1110+32del
XM_011544803.1:c.1350+32del	XP_011543105.1:n.1350+32del
XM_011544804.1:c.1350+32del	XP_011543106.1:n.1350+32del
XM_011544805.1:c.1350+32del	XP_011543107.1:n.1350+32del
XM_011544806.1:c.1350+32del	XP_011543108.1:n.1350+32del
XM_011544807.1:c.654+32del	XP_011543109.1:n.654+32del
XM_011544808.1:c.519+32del	XP_011543110.1:n.519+32del
XR_247191.1:n.1451+32del
XM_005273824.4:c.1347+32del	XP_005273881.1:n.1347+32del
XM_005273826.4:c.1095+32del	XP_005273883.1:n.1095+32del
XM_005273830.4:c.657+32del	XP_005273887.1:n.657+32del
XM_005273831.4:c.657+32del	XP_005273888.1:n.657+32del
XM_005273832.4:c.627+32del	XP_005273889.1:n.627+32del
XM_011544802.3:c.1110+32del	XP_011543104.1:n.1110+32del
XM_011544807.3:c.654+32del	XP_011543109.1:n.654+32del
XM_011544808.3:c.519+32del	XP_011543110.1:n.519+32del
XM_017017328.2:c.1181+32del	XP_016872817.1:n.1181+32del
XM_017017329.2:c.1178+32del	XP_016872818.1:n.1178+32del
XM_017017330.2:c.627+32del	XP_016872819.1:n.627+32del
XM_017017331.2:c.627+32del	XP_016872820.1:n.627+32del
XM_017017332.2:c.441+32del	XP_016872821.1:n.441+32del
XM_017017333.2:c.458+32del	XP_016872822.1:n.458+32del
XM_017017334.2:c.458+32del	XP_016872823.1:n.458+32del
XM_017017335.2:c.458+32del	XP_016872824.1:n.458+32del
XM_017017336.2:c.350+32del	XP_016872825.1:n.350+32del
XM_024448392.1:c.1140+32del	XP_024304160.1:n.1140+32del
XM_024448393.1:c.627+32del	XP_024304161.1:n.627+32del
XR_001747789.2:n.1282+32del
XR_001747790.2:n.1282+32del
XR_247191.3:n.1454+32del
NM_139075.4:c.1350+32del MANE Select	NP_620714.2:n.1350+32del