Canonical Allele Identifier: CA2497029811
Gene: TPCN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69087895G= , CM000673.2:g.69087895G= GRCh38
NC_000011.9:g.68855363G= , CM000673.1:g.68855363G= GRCh37
NC_000011.8:g.68611939G= NCBI36
NG_016153.1:g.44014G=

Transcript Alleles

HGVS Amino-acid change
ENST00000692585.1:c.1058G= ENSP00000509200.1:p.Gly353=
ENST00000294309.8:c.2201G= MANE Select ENSP00000294309.3:p.Gly734=
ENST00000635811.1:c.*396G= ENSP00000490341.1:n.*396G=
ENST00000637084.1:c.1058G= ENSP00000490615.1:p.Gly353=
ENST00000637342.1:c.2003+1965G= ENSP00000490171.1:n.2003+1965G=
ENST00000637504.1:c.*33+2609G= ENSP00000489759.1:n.*33+2609G=
ENST00000294309.7:c.2201G= ENSP00000294309.3:p.Gly734=
ENST00000442692.2:n.1667G=
ENST00000542467.1:c.1655G= ENSP00000445551.1:p.Gly552=
NM_139075.3:c.2201G= NP_620714.2:p.Gly734=
XM_005273824.2:c.2198G= XP_005273881.1:p.Gly733=
XM_005273826.2:c.1946G= XP_005273883.1:p.Gly649=
XM_005273830.2:c.1508G= XP_005273887.1:p.Gly503=
XM_005273831.2:c.1508G= XP_005273888.1:p.Gly503=
XM_005273832.2:c.1478G= XP_005273889.1:p.Gly493=
XM_006718453.2:c.1639+6396G= XP_006718516.1:n.1639+6396G=
XM_006718454.2:c.1689+6396G= XP_006718517.1:n.1689+6396G=
XM_011544802.1:c.1961G= XP_011543104.1:p.Gly654=
XM_011544807.1:c.1505G= XP_011543109.1:p.Gly502=
XM_011544808.1:c.1370G= XP_011543110.1:p.Gly457=
XR_247191.1:n.2252G=
XM_005273824.4:c.2198G= XP_005273881.1:p.Gly733=
XM_005273826.4:c.1946G= XP_005273883.1:p.Gly649=
XM_005273830.4:c.1508G= XP_005273887.1:p.Gly503=
XM_005273831.4:c.1508G= XP_005273888.1:p.Gly503=
XM_005273832.4:c.1478G= XP_005273889.1:p.Gly493=
XM_011544802.3:c.1961G= XP_011543104.1:p.Gly654=
XM_011544807.3:c.1505G= XP_011543109.1:p.Gly502=
XM_011544808.3:c.1370G= XP_011543110.1:p.Gly457=
XM_017017328.2:c.1982G= XP_016872817.1:p.Gly661=
XM_017017329.2:c.1979G= XP_016872818.1:p.Gly660=
XM_017017330.2:c.1478G= XP_016872819.1:p.Gly493=
XM_017017331.2:c.1478G= XP_016872820.1:p.Gly493=
XM_017017332.2:c.1292G= XP_016872821.1:p.Gly431=
XM_017017333.2:c.1259G= XP_016872822.1:p.Gly420=
XM_017017334.2:c.1259G= XP_016872823.1:p.Gly420=
XM_017017335.2:c.1259G= XP_016872824.1:p.Gly420=
XM_017017336.2:c.1151G= XP_016872825.1:p.Gly384=
XM_024448392.1:c.1991G= XP_024304160.1:p.Gly664=
XM_024448393.1:c.1478G= XP_024304161.1:p.Gly493=
XR_001747789.2:n.2133G=
XR_247191.3:n.2255G=
NM_139075.4:c.2201G= MANE Select NP_620714.2:p.Gly734=