Canonical Allele Identifier: CA2614769710

Gene: TPCN2

Linked Data

• gnomAD v4: 11-69088063-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69088063_69088064insC , CM000673.2:g.69088063_69088064insC	GRCh38
NC_000011.9:g.68855531_68855532insC , CM000673.1:g.68855531_68855532insC	GRCh37
NC_000011.8:g.68612107_68612108insC	NCBI36
NG_016153.1:g.44182_44183insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000692585.1:c.1226_1227insC	ENSP00000509200.1:n.1226_1227insC
ENST00000294309.8:c.*110_*111insC MANE Select	ENSP00000294309.3:n.*110_*111insC
ENST00000635811.1:c.*564_*565insC	ENSP00000490341.1:n.*564_*565insC
ENST00000637084.1:c.1226_1227insC	ENSP00000490615.1:n.1226_1227insC
ENST00000637342.1:c.2003+2133_2003+2134insC	ENSP00000490171.1:n.2003+2133_2003+2134insC
ENST00000637504.1:c.*33+2777_*33+2778insC	ENSP00000489759.1:n.*33+2777_*33+2778insC
ENST00000294309.7:c.*110_*111insC	ENSP00000294309.3:n.*110_*111insC
ENST00000442692.2:n.1835_1836insC
ENST00000542467.1:c.*110_*111insC	ENSP00000445551.1:n.*110_*111insC
NM_139075.3:c.*110_*111insC	NP_620714.2:n.*110_*111insC
XM_005273824.2:c.*110_*111insC	XP_005273881.1:n.*110_*111insC
XM_005273826.2:c.*110_*111insC	XP_005273883.1:n.*110_*111insC
XM_005273830.2:c.*110_*111insC	XP_005273887.1:n.*110_*111insC
XM_005273831.2:c.*110_*111insC	XP_005273888.1:n.*110_*111insC
XM_005273832.2:c.*110_*111insC	XP_005273889.1:n.*110_*111insC
XM_006718453.2:c.1639+6564_1639+6565insC	XP_006718516.1:n.1639+6564_1639+6565insC
XM_006718454.2:c.1689+6564_1689+6565insC	XP_006718517.1:n.1689+6564_1689+6565insC
XM_011544802.1:c.*110_*111insC	XP_011543104.1:n.*110_*111insC
XM_011544807.1:c.*110_*111insC	XP_011543109.1:n.*110_*111insC
XM_011544808.1:c.*110_*111insC	XP_011543110.1:n.*110_*111insC
XM_005273824.4:c.*110_*111insC	XP_005273881.1:n.*110_*111insC
XM_005273826.4:c.*110_*111insC	XP_005273883.1:n.*110_*111insC
XM_005273830.4:c.*110_*111insC	XP_005273887.1:n.*110_*111insC
XM_005273831.4:c.*110_*111insC	XP_005273888.1:n.*110_*111insC
XM_005273832.4:c.*110_*111insC	XP_005273889.1:n.*110_*111insC
XM_011544802.3:c.*110_*111insC	XP_011543104.1:n.*110_*111insC
XM_011544807.3:c.*110_*111insC	XP_011543109.1:n.*110_*111insC
XM_011544808.3:c.*110_*111insC	XP_011543110.1:n.*110_*111insC
XM_017017328.2:c.*110_*111insC	XP_016872817.1:n.*110_*111insC
XM_017017329.2:c.*110_*111insC	XP_016872818.1:n.*110_*111insC
XM_017017330.2:c.*110_*111insC	XP_016872819.1:n.*110_*111insC
XM_017017331.2:c.*110_*111insC	XP_016872820.1:n.*110_*111insC
XM_017017332.2:c.*110_*111insC	XP_016872821.1:n.*110_*111insC
XM_017017333.2:c.*110_*111insC	XP_016872822.1:n.*110_*111insC
XM_017017334.2:c.*110_*111insC	XP_016872823.1:n.*110_*111insC
XM_017017335.2:c.*110_*111insC	XP_016872824.1:n.*110_*111insC
XM_017017336.2:c.*110_*111insC	XP_016872825.1:n.*110_*111insC
XM_024448392.1:c.*110_*111insC	XP_024304160.1:n.*110_*111insC
XM_024448393.1:c.*110_*111insC	XP_024304161.1:n.*110_*111insC
XR_001747789.2:n.2301_2302insC
XR_247191.3:n.2423_2424insC
NM_139075.4:c.*110_*111insC MANE Select	NP_620714.2:n.*110_*111insC