Canonical Allele Identifier: CA381656494

Gene: TPCN2

Linked Data

• MyVariant Identifiers: chr11:g.68846459T>G (hg19) ; chr11:g.69078991T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69078991T>G , CM000673.2:g.69078991T>G	GRCh38
NC_000011.9:g.68846459T>G , CM000673.1:g.68846459T>G	GRCh37
NC_000011.8:g.68603035T>G	NCBI36
NG_016153.1:g.35110T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000692585.1:c.367T>G	ENSP00000509200.1:p.Phe123Val
ENST00000294309.8:c.1510T>G MANE Select	ENSP00000294309.3:p.Phe504Val
ENST00000635811.1:c.1510T>G	ENSP00000490341.1:p.Phe504Val
ENST00000637084.1:c.367T>G	ENSP00000490615.1:p.Phe123Val
ENST00000637342.1:c.1510T>G	ENSP00000490171.1:p.Phe504Val
ENST00000637504.1:c.1510T>G	ENSP00000489759.1:p.Phe504Val
ENST00000294309.7:c.1510T>G	ENSP00000294309.3:p.Phe504Val
ENST00000442692.2:n.1103T>G
ENST00000535009.5:n.1319T>G
ENST00000542467.1:c.1510T>G	ENSP00000445551.1:p.Phe504Val
NM_139075.3:c.1510T>G	NP_620714.2:p.Phe504Val
XM_005273824.2:c.1507T>G	XP_005273881.1:p.Phe503Val
XM_005273826.2:c.1255T>G	XP_005273883.1:p.Phe419Val
XM_005273827.2:c.1510T>G	XP_005273884.1:p.Phe504Val
XM_005273828.2:c.1510T>G	XP_005273885.1:p.Phe504Val
XM_005273830.2:c.817T>G	XP_005273887.1:p.Phe273Val
XM_005273831.2:c.817T>G	XP_005273888.1:p.Phe273Val
XM_005273832.2:c.787T>G	XP_005273889.1:p.Phe263Val
XM_006718453.2:c.1510T>G	XP_006718516.1:p.Phe504Val
XM_006718454.2:c.1510T>G	XP_006718517.1:p.Phe504Val
XM_006718456.2:c.1510T>G	XP_006718519.1:p.Phe504Val
XM_011544802.1:c.1270T>G	XP_011543104.1:p.Phe424Val
XM_011544803.1:c.1510T>G	XP_011543105.1:p.Phe504Val
XM_011544804.1:c.1510T>G	XP_011543106.1:p.Phe504Val
XM_011544805.1:c.1510T>G	XP_011543107.1:p.Phe504Val
XM_011544806.1:c.1510T>G	XP_011543108.1:p.Phe504Val
XM_011544807.1:c.814T>G	XP_011543109.1:p.Phe272Val
XM_011544808.1:c.679T>G	XP_011543110.1:p.Phe227Val
XR_247191.1:n.1611T>G
XM_005273824.4:c.1507T>G	XP_005273881.1:p.Phe503Val
XM_005273826.4:c.1255T>G	XP_005273883.1:p.Phe419Val
XM_005273830.4:c.817T>G	XP_005273887.1:p.Phe273Val
XM_005273831.4:c.817T>G	XP_005273888.1:p.Phe273Val
XM_005273832.4:c.787T>G	XP_005273889.1:p.Phe263Val
XM_011544802.3:c.1270T>G	XP_011543104.1:p.Phe424Val
XM_011544807.3:c.814T>G	XP_011543109.1:p.Phe272Val
XM_011544808.3:c.679T>G	XP_011543110.1:p.Phe227Val
XM_017017328.2:c.1341T>G	XP_016872817.1:p.Cys447Trp
XM_017017329.2:c.1338T>G	XP_016872818.1:p.Cys446Trp
XM_017017330.2:c.787T>G	XP_016872819.1:p.Phe263Val
XM_017017331.2:c.787T>G	XP_016872820.1:p.Phe263Val
XM_017017332.2:c.601T>G	XP_016872821.1:p.Phe201Val
XM_017017333.2:c.618T>G	XP_016872822.1:p.Cys206Trp
XM_017017334.2:c.618T>G	XP_016872823.1:p.Cys206Trp
XM_017017335.2:c.618T>G	XP_016872824.1:p.Cys206Trp
XM_017017336.2:c.510T>G	XP_016872825.1:p.Cys170Trp
XM_024448392.1:c.1300T>G	XP_024304160.1:p.Phe434Val
XM_024448393.1:c.787T>G	XP_024304161.1:p.Phe263Val
XR_001747789.2:n.1442T>G
XR_001747790.2:n.1442T>G
XR_247191.3:n.1614T>G
NM_139075.4:c.1510T>G MANE Select	NP_620714.2:p.Phe504Val