Canonical Allele Identifier: CA381655920

Gene: TPCN2

Linked Data

• MyVariant Identifiers: chr11:g.68846227T>A (hg19) ; chr11:g.69078759T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69078759T>A , CM000673.2:g.69078759T>A	GRCh38
NC_000011.9:g.68846227T>A , CM000673.1:g.68846227T>A	GRCh37
NC_000011.8:g.68602803T>A	NCBI36
NG_016153.1:g.34878T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000692585.1:c.233T>A	ENSP00000509200.1:p.Val78Glu
ENST00000294309.8:c.1376T>A MANE Select	ENSP00000294309.3:p.Val459Glu
ENST00000635811.1:c.1376T>A	ENSP00000490341.1:p.Val459Glu
ENST00000637084.1:c.233T>A	ENSP00000490615.1:p.Val78Glu
ENST00000637342.1:c.1376T>A	ENSP00000490171.1:p.Val459Glu
ENST00000637504.1:c.1376T>A	ENSP00000489759.1:p.Val459Glu
ENST00000294309.7:c.1376T>A	ENSP00000294309.3:p.Val459Glu
ENST00000442692.2:n.969T>A
ENST00000535009.5:n.1185T>A
ENST00000542467.1:c.1376T>A	ENSP00000445551.1:p.Val459Glu
NM_139075.3:c.1376T>A	NP_620714.2:p.Val459Glu
XM_005273824.2:c.1373T>A	XP_005273881.1:p.Val458Glu
XM_005273826.2:c.1121T>A	XP_005273883.1:p.Val374Glu
XM_005273827.2:c.1376T>A	XP_005273884.1:p.Val459Glu
XM_005273828.2:c.1376T>A	XP_005273885.1:p.Val459Glu
XM_005273830.2:c.683T>A	XP_005273887.1:p.Val228Glu
XM_005273831.2:c.683T>A	XP_005273888.1:p.Val228Glu
XM_005273832.2:c.653T>A	XP_005273889.1:p.Val218Glu
XM_006718453.2:c.1376T>A	XP_006718516.1:p.Val459Glu
XM_006718454.2:c.1376T>A	XP_006718517.1:p.Val459Glu
XM_006718456.2:c.1376T>A	XP_006718519.1:p.Val459Glu
XM_011544802.1:c.1136T>A	XP_011543104.1:p.Val379Glu
XM_011544803.1:c.1376T>A	XP_011543105.1:p.Val459Glu
XM_011544804.1:c.1376T>A	XP_011543106.1:p.Val459Glu
XM_011544805.1:c.1376T>A	XP_011543107.1:p.Val459Glu
XM_011544806.1:c.1376T>A	XP_011543108.1:p.Val459Glu
XM_011544807.1:c.680T>A	XP_011543109.1:p.Val227Glu
XM_011544808.1:c.545T>A	XP_011543110.1:p.Val182Glu
XR_247191.1:n.1477T>A
XM_005273824.4:c.1373T>A	XP_005273881.1:p.Val458Glu
XM_005273826.4:c.1121T>A	XP_005273883.1:p.Val374Glu
XM_005273830.4:c.683T>A	XP_005273887.1:p.Val228Glu
XM_005273831.4:c.683T>A	XP_005273888.1:p.Val228Glu
XM_005273832.4:c.653T>A	XP_005273889.1:p.Val218Glu
XM_011544802.3:c.1136T>A	XP_011543104.1:p.Val379Glu
XM_011544807.3:c.680T>A	XP_011543109.1:p.Val227Glu
XM_011544808.3:c.545T>A	XP_011543110.1:p.Val182Glu
XM_017017328.2:c.1207T>A	XP_016872817.1:p.Cys403Ser
XM_017017329.2:c.1204T>A	XP_016872818.1:p.Cys402Ser
XM_017017330.2:c.653T>A	XP_016872819.1:p.Val218Glu
XM_017017331.2:c.653T>A	XP_016872820.1:p.Val218Glu
XM_017017332.2:c.467T>A	XP_016872821.1:p.Val156Glu
XM_017017333.2:c.484T>A	XP_016872822.1:p.Cys162Ser
XM_017017334.2:c.484T>A	XP_016872823.1:p.Cys162Ser
XM_017017335.2:c.484T>A	XP_016872824.1:p.Cys162Ser
XM_017017336.2:c.376T>A	XP_016872825.1:p.Cys126Ser
XM_024448392.1:c.1166T>A	XP_024304160.1:p.Val389Glu
XM_024448393.1:c.653T>A	XP_024304161.1:p.Val218Glu
XR_001747789.2:n.1308T>A
XR_001747790.2:n.1308T>A
XR_247191.3:n.1480T>A
NM_139075.4:c.1376T>A MANE Select	NP_620714.2:p.Val459Glu