Canonical Allele Identifier: CA2614769755

Gene: TPCN2

Linked Data

• gnomAD v4: 11-69088092-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69088092C>T , CM000673.2:g.69088092C>T	GRCh38
NC_000011.9:g.68855560C>T , CM000673.1:g.68855560C>T	GRCh37
NC_000011.8:g.68612136C>T	NCBI36
NG_016153.1:g.44211C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000692585.1:c.1255C>T	ENSP00000509200.1:n.1255C>T
ENST00000294309.8:c.*139C>T MANE Select	ENSP00000294309.3:n.*139C>T
ENST00000635811.1:c.*593C>T	ENSP00000490341.1:n.*593C>T
ENST00000637084.1:c.1255C>T	ENSP00000490615.1:n.1255C>T
ENST00000637342.1:c.2003+2162C>T	ENSP00000490171.1:n.2003+2162C>T
ENST00000637504.1:c.*33+2806C>T	ENSP00000489759.1:n.*33+2806C>T
ENST00000294309.7:c.*139C>T	ENSP00000294309.3:n.*139C>T
ENST00000442692.2:n.1864C>T
ENST00000542467.1:c.*139C>T	ENSP00000445551.1:n.*139C>T
NM_139075.3:c.*139C>T	NP_620714.2:n.*139C>T
XM_005273824.2:c.*139C>T	XP_005273881.1:n.*139C>T
XM_005273826.2:c.*139C>T	XP_005273883.1:n.*139C>T
XM_005273830.2:c.*139C>T	XP_005273887.1:n.*139C>T
XM_005273831.2:c.*139C>T	XP_005273888.1:n.*139C>T
XM_005273832.2:c.*139C>T	XP_005273889.1:n.*139C>T
XM_006718453.2:c.1639+6593C>T	XP_006718516.1:n.1639+6593C>T
XM_006718454.2:c.1689+6593C>T	XP_006718517.1:n.1689+6593C>T
XM_011544802.1:c.*139C>T	XP_011543104.1:n.*139C>T
XM_011544807.1:c.*139C>T	XP_011543109.1:n.*139C>T
XM_011544808.1:c.*139C>T	XP_011543110.1:n.*139C>T
XM_005273824.4:c.*139C>T	XP_005273881.1:n.*139C>T
XM_005273826.4:c.*139C>T	XP_005273883.1:n.*139C>T
XM_005273830.4:c.*139C>T	XP_005273887.1:n.*139C>T
XM_005273831.4:c.*139C>T	XP_005273888.1:n.*139C>T
XM_005273832.4:c.*139C>T	XP_005273889.1:n.*139C>T
XM_011544802.3:c.*139C>T	XP_011543104.1:n.*139C>T
XM_011544807.3:c.*139C>T	XP_011543109.1:n.*139C>T
XM_011544808.3:c.*139C>T	XP_011543110.1:n.*139C>T
XM_017017328.2:c.*139C>T	XP_016872817.1:n.*139C>T
XM_017017329.2:c.*139C>T	XP_016872818.1:n.*139C>T
XM_017017330.2:c.*139C>T	XP_016872819.1:n.*139C>T
XM_017017331.2:c.*139C>T	XP_016872820.1:n.*139C>T
XM_017017332.2:c.*139C>T	XP_016872821.1:n.*139C>T
XM_017017333.2:c.*139C>T	XP_016872822.1:n.*139C>T
XM_017017334.2:c.*139C>T	XP_016872823.1:n.*139C>T
XM_017017335.2:c.*139C>T	XP_016872824.1:n.*139C>T
XM_017017336.2:c.*139C>T	XP_016872825.1:n.*139C>T
XM_024448392.1:c.*139C>T	XP_024304160.1:n.*139C>T
XM_024448393.1:c.*139C>T	XP_024304161.1:n.*139C>T
XR_001747789.2:n.2330C>T
XR_247191.3:n.2452C>T
NM_139075.4:c.*139C>T MANE Select	NP_620714.2:n.*139C>T