Canonical Allele Identifier: CA2581029364
Gene: TPCN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69078630A= , CM000673.2:g.69078630A= GRCh38
NC_000011.9:g.68846098A= , CM000673.1:g.68846098A= GRCh37
NC_000011.8:g.68602674A= NCBI36
NG_016153.1:g.34749A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000692585.1:c.207+29A= ENSP00000509200.1:n.207+29A=
ENST00000294309.8:c.1350+29A= MANE Select ENSP00000294309.3:n.1350+29A=
ENST00000635811.1:c.1350+29A= ENSP00000490341.1:n.1350+29A=
ENST00000637084.1:c.207+29A= ENSP00000490615.1:n.207+29A=
ENST00000637342.1:c.1350+29A= ENSP00000490171.1:n.1350+29A=
ENST00000637504.1:c.1350+29A= ENSP00000489759.1:n.1350+29A=
ENST00000294309.7:c.1350+29A= ENSP00000294309.3:n.1350+29A=
ENST00000442692.2:n.943+29A=
ENST00000535009.5:n.1159+29A=
ENST00000542467.1:c.1350+29A= ENSP00000445551.1:n.1350+29A=
NM_139075.3:c.1350+29A= NP_620714.2:n.1350+29A=
XM_005273824.2:c.1347+29A= XP_005273881.1:n.1347+29A=
XM_005273826.2:c.1095+29A= XP_005273883.1:n.1095+29A=
XM_005273827.2:c.1350+29A= XP_005273884.1:n.1350+29A=
XM_005273828.2:c.1350+29A= XP_005273885.1:n.1350+29A=
XM_005273830.2:c.657+29A= XP_005273887.1:n.657+29A=
XM_005273831.2:c.657+29A= XP_005273888.1:n.657+29A=
XM_005273832.2:c.627+29A= XP_005273889.1:n.627+29A=
XM_006718453.2:c.1350+29A= XP_006718516.1:n.1350+29A=
XM_006718454.2:c.1350+29A= XP_006718517.1:n.1350+29A=
XM_006718456.2:c.1350+29A= XP_006718519.1:n.1350+29A=
XM_011544802.1:c.1110+29A= XP_011543104.1:n.1110+29A=
XM_011544803.1:c.1350+29A= XP_011543105.1:n.1350+29A=
XM_011544804.1:c.1350+29A= XP_011543106.1:n.1350+29A=
XM_011544805.1:c.1350+29A= XP_011543107.1:n.1350+29A=
XM_011544806.1:c.1350+29A= XP_011543108.1:n.1350+29A=
XM_011544807.1:c.654+29A= XP_011543109.1:n.654+29A=
XM_011544808.1:c.519+29A= XP_011543110.1:n.519+29A=
XR_247191.1:n.1451+29A=
XM_005273824.4:c.1347+29A= XP_005273881.1:n.1347+29A=
XM_005273826.4:c.1095+29A= XP_005273883.1:n.1095+29A=
XM_005273830.4:c.657+29A= XP_005273887.1:n.657+29A=
XM_005273831.4:c.657+29A= XP_005273888.1:n.657+29A=
XM_005273832.4:c.627+29A= XP_005273889.1:n.627+29A=
XM_011544802.3:c.1110+29A= XP_011543104.1:n.1110+29A=
XM_011544807.3:c.654+29A= XP_011543109.1:n.654+29A=
XM_011544808.3:c.519+29A= XP_011543110.1:n.519+29A=
XM_017017328.2:c.1181+29A= XP_016872817.1:n.1181+29A=
XM_017017329.2:c.1178+29A= XP_016872818.1:n.1178+29A=
XM_017017330.2:c.627+29A= XP_016872819.1:n.627+29A=
XM_017017331.2:c.627+29A= XP_016872820.1:n.627+29A=
XM_017017332.2:c.441+29A= XP_016872821.1:n.441+29A=
XM_017017333.2:c.458+29A= XP_016872822.1:n.458+29A=
XM_017017334.2:c.458+29A= XP_016872823.1:n.458+29A=
XM_017017335.2:c.458+29A= XP_016872824.1:n.458+29A=
XM_017017336.2:c.350+29A= XP_016872825.1:n.350+29A=
XM_024448392.1:c.1140+29A= XP_024304160.1:n.1140+29A=
XM_024448393.1:c.627+29A= XP_024304161.1:n.627+29A=
XR_001747789.2:n.1282+29A=
XR_001747790.2:n.1282+29A=
XR_247191.3:n.1454+29A=
NM_139075.4:c.1350+29A= MANE Select NP_620714.2:n.1350+29A=