Canonical Allele Identifier: CA2574905822

Gene: TPCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69087848T>C , CM000673.2:g.69087848T>C	GRCh38
NC_000011.9:g.68855316T>C , CM000673.1:g.68855316T>C	GRCh37
NC_000011.8:g.68611892T>C	NCBI36
NG_016153.1:g.43967T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000692585.1:c.1038-27T>C	ENSP00000509200.1:n.1038-27T>C
ENST00000294309.8:c.2181-27T>C MANE Select	ENSP00000294309.3:n.2181-27T>C
ENST00000635811.1:c.*376-27T>C	ENSP00000490341.1:n.*376-27T>C
ENST00000637084.1:c.1038-27T>C	ENSP00000490615.1:n.1038-27T>C
ENST00000637342.1:c.2003+1918T>C	ENSP00000490171.1:n.2003+1918T>C
ENST00000637504.1:c.*33+2562T>C	ENSP00000489759.1:n.*33+2562T>C
ENST00000294309.7:c.2181-27T>C	ENSP00000294309.3:n.2181-27T>C
ENST00000442692.2:n.1647-27T>C
ENST00000542467.1:c.1635-27T>C	ENSP00000445551.1:n.1635-27T>C
NM_139075.3:c.2181-27T>C	NP_620714.2:n.2181-27T>C
XM_005273824.2:c.2178-27T>C	XP_005273881.1:n.2178-27T>C
XM_005273826.2:c.1926-27T>C	XP_005273883.1:n.1926-27T>C
XM_005273830.2:c.1488-27T>C	XP_005273887.1:n.1488-27T>C
XM_005273831.2:c.1488-27T>C	XP_005273888.1:n.1488-27T>C
XM_005273832.2:c.1458-27T>C	XP_005273889.1:n.1458-27T>C
XM_006718453.2:c.1639+6349T>C	XP_006718516.1:n.1639+6349T>C
XM_006718454.2:c.1689+6349T>C	XP_006718517.1:n.1689+6349T>C
XM_011544802.1:c.1941-27T>C	XP_011543104.1:n.1941-27T>C
XM_011544807.1:c.1485-27T>C	XP_011543109.1:n.1485-27T>C
XM_011544808.1:c.1350-27T>C	XP_011543110.1:n.1350-27T>C
XR_247191.1:n.2232-27T>C
XM_005273824.4:c.2178-27T>C	XP_005273881.1:n.2178-27T>C
XM_005273826.4:c.1926-27T>C	XP_005273883.1:n.1926-27T>C
XM_005273830.4:c.1488-27T>C	XP_005273887.1:n.1488-27T>C
XM_005273831.4:c.1488-27T>C	XP_005273888.1:n.1488-27T>C
XM_005273832.4:c.1458-27T>C	XP_005273889.1:n.1458-27T>C
XM_011544802.3:c.1941-27T>C	XP_011543104.1:n.1941-27T>C
XM_011544807.3:c.1485-27T>C	XP_011543109.1:n.1485-27T>C
XM_011544808.3:c.1350-27T>C	XP_011543110.1:n.1350-27T>C
XM_017017328.2:c.1962-27T>C	XP_016872817.1:n.1962-27T>C
XM_017017329.2:c.1959-27T>C	XP_016872818.1:n.1959-27T>C
XM_017017330.2:c.1458-27T>C	XP_016872819.1:n.1458-27T>C
XM_017017331.2:c.1458-27T>C	XP_016872820.1:n.1458-27T>C
XM_017017332.2:c.1272-27T>C	XP_016872821.1:n.1272-27T>C
XM_017017333.2:c.1239-27T>C	XP_016872822.1:n.1239-27T>C
XM_017017334.2:c.1239-27T>C	XP_016872823.1:n.1239-27T>C
XM_017017335.2:c.1239-27T>C	XP_016872824.1:n.1239-27T>C
XM_017017336.2:c.1131-27T>C	XP_016872825.1:n.1131-27T>C
XM_024448392.1:c.1971-27T>C	XP_024304160.1:n.1971-27T>C
XM_024448393.1:c.1458-27T>C	XP_024304161.1:n.1458-27T>C
XR_001747789.2:n.2113-27T>C
XR_247191.3:n.2235-27T>C
NM_139075.4:c.2181-27T>C MANE Select	NP_620714.2:n.2181-27T>C