Canonical Allele Identifier: CA381656342

Gene: TPCN2

Linked Data

• MyVariant Identifiers: chr11:g.68846424G>T (hg19) ; chr11:g.69078956G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69078956G>T , CM000673.2:g.69078956G>T	GRCh38
NC_000011.9:g.68846424G>T , CM000673.1:g.68846424G>T	GRCh37
NC_000011.8:g.68603000G>T	NCBI36
NG_016153.1:g.35075G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000692585.1:c.332G>T	ENSP00000509200.1:p.Gly111Val
ENST00000294309.8:c.1475G>T MANE Select	ENSP00000294309.3:p.Gly492Val
ENST00000635811.1:c.1475G>T	ENSP00000490341.1:p.Gly492Val
ENST00000637084.1:c.332G>T	ENSP00000490615.1:p.Gly111Val
ENST00000637342.1:c.1475G>T	ENSP00000490171.1:p.Gly492Val
ENST00000637504.1:c.1475G>T	ENSP00000489759.1:p.Gly492Val
ENST00000294309.7:c.1475G>T	ENSP00000294309.3:p.Gly492Val
ENST00000442692.2:n.1068G>T
ENST00000535009.5:n.1284G>T
ENST00000542467.1:c.1475G>T	ENSP00000445551.1:p.Gly492Val
NM_139075.3:c.1475G>T	NP_620714.2:p.Gly492Val
XM_005273824.2:c.1472G>T	XP_005273881.1:p.Gly491Val
XM_005273826.2:c.1220G>T	XP_005273883.1:p.Gly407Val
XM_005273827.2:c.1475G>T	XP_005273884.1:p.Gly492Val
XM_005273828.2:c.1475G>T	XP_005273885.1:p.Gly492Val
XM_005273830.2:c.782G>T	XP_005273887.1:p.Gly261Val
XM_005273831.2:c.782G>T	XP_005273888.1:p.Gly261Val
XM_005273832.2:c.752G>T	XP_005273889.1:p.Gly251Val
XM_006718453.2:c.1475G>T	XP_006718516.1:p.Gly492Val
XM_006718454.2:c.1475G>T	XP_006718517.1:p.Gly492Val
XM_006718456.2:c.1475G>T	XP_006718519.1:p.Gly492Val
XM_011544802.1:c.1235G>T	XP_011543104.1:p.Gly412Val
XM_011544803.1:c.1475G>T	XP_011543105.1:p.Gly492Val
XM_011544804.1:c.1475G>T	XP_011543106.1:p.Gly492Val
XM_011544805.1:c.1475G>T	XP_011543107.1:p.Gly492Val
XM_011544806.1:c.1475G>T	XP_011543108.1:p.Gly492Val
XM_011544807.1:c.779G>T	XP_011543109.1:p.Gly260Val
XM_011544808.1:c.644G>T	XP_011543110.1:p.Gly215Val
XR_247191.1:n.1576G>T
XM_005273824.4:c.1472G>T	XP_005273881.1:p.Gly491Val
XM_005273826.4:c.1220G>T	XP_005273883.1:p.Gly407Val
XM_005273830.4:c.782G>T	XP_005273887.1:p.Gly261Val
XM_005273831.4:c.782G>T	XP_005273888.1:p.Gly261Val
XM_005273832.4:c.752G>T	XP_005273889.1:p.Gly251Val
XM_011544802.3:c.1235G>T	XP_011543104.1:p.Gly412Val
XM_011544807.3:c.779G>T	XP_011543109.1:p.Gly260Val
XM_011544808.3:c.644G>T	XP_011543110.1:p.Gly215Val
XM_017017328.2:c.1306G>T	XP_016872817.1:p.Ala436Ser
XM_017017329.2:c.1303G>T	XP_016872818.1:p.Ala435Ser
XM_017017330.2:c.752G>T	XP_016872819.1:p.Gly251Val
XM_017017331.2:c.752G>T	XP_016872820.1:p.Gly251Val
XM_017017332.2:c.566G>T	XP_016872821.1:p.Gly189Val
XM_017017333.2:c.583G>T	XP_016872822.1:p.Ala195Ser
XM_017017334.2:c.583G>T	XP_016872823.1:p.Ala195Ser
XM_017017335.2:c.583G>T	XP_016872824.1:p.Ala195Ser
XM_017017336.2:c.475G>T	XP_016872825.1:p.Ala159Ser
XM_024448392.1:c.1265G>T	XP_024304160.1:p.Gly422Val
XM_024448393.1:c.752G>T	XP_024304161.1:p.Gly251Val
XR_001747789.2:n.1407G>T
XR_001747790.2:n.1407G>T
XR_247191.3:n.1579G>T
NM_139075.4:c.1475G>T MANE Select	NP_620714.2:p.Gly492Val