Canonical Allele Identifier: CA381652117

Gene: TPCN2

Linked Data

• MyVariant Identifiers: chr11:g.68855359C>T (hg19) ; chr11:g.69087891C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69087891C>T , CM000673.2:g.69087891C>T	GRCh38
NC_000011.9:g.68855359C>T , CM000673.1:g.68855359C>T	GRCh37
NC_000011.8:g.68611935C>T	NCBI36
NG_016153.1:g.44010C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000692585.1:c.1054C>T	ENSP00000509200.1:p.Pro352Ser
ENST00000294309.8:c.2197C>T MANE Select	ENSP00000294309.3:p.Pro733Ser
ENST00000635811.1:c.*392C>T	ENSP00000490341.1:n.*392C>T
ENST00000637084.1:c.1054C>T	ENSP00000490615.1:p.Pro352Ser
ENST00000637342.1:c.2003+1961C>T	ENSP00000490171.1:n.2003+1961C>T
ENST00000637504.1:c.*33+2605C>T	ENSP00000489759.1:n.*33+2605C>T
ENST00000294309.7:c.2197C>T	ENSP00000294309.3:p.Pro733Ser
ENST00000442692.2:n.1663C>T
ENST00000542467.1:c.1651C>T	ENSP00000445551.1:p.Pro551Ser
NM_139075.3:c.2197C>T	NP_620714.2:p.Pro733Ser
XM_005273824.2:c.2194C>T	XP_005273881.1:p.Pro732Ser
XM_005273826.2:c.1942C>T	XP_005273883.1:p.Pro648Ser
XM_005273830.2:c.1504C>T	XP_005273887.1:p.Pro502Ser
XM_005273831.2:c.1504C>T	XP_005273888.1:p.Pro502Ser
XM_005273832.2:c.1474C>T	XP_005273889.1:p.Pro492Ser
XM_006718453.2:c.1639+6392C>T	XP_006718516.1:n.1639+6392C>T
XM_006718454.2:c.1689+6392C>T	XP_006718517.1:n.1689+6392C>T
XM_011544802.1:c.1957C>T	XP_011543104.1:p.Pro653Ser
XM_011544807.1:c.1501C>T	XP_011543109.1:p.Pro501Ser
XM_011544808.1:c.1366C>T	XP_011543110.1:p.Pro456Ser
XR_247191.1:n.2248C>T
XM_005273824.4:c.2194C>T	XP_005273881.1:p.Pro732Ser
XM_005273826.4:c.1942C>T	XP_005273883.1:p.Pro648Ser
XM_005273830.4:c.1504C>T	XP_005273887.1:p.Pro502Ser
XM_005273831.4:c.1504C>T	XP_005273888.1:p.Pro502Ser
XM_005273832.4:c.1474C>T	XP_005273889.1:p.Pro492Ser
XM_011544802.3:c.1957C>T	XP_011543104.1:p.Pro653Ser
XM_011544807.3:c.1501C>T	XP_011543109.1:p.Pro501Ser
XM_011544808.3:c.1366C>T	XP_011543110.1:p.Pro456Ser
XM_017017328.2:c.1978C>T	XP_016872817.1:p.Pro660Ser
XM_017017329.2:c.1975C>T	XP_016872818.1:p.Pro659Ser
XM_017017330.2:c.1474C>T	XP_016872819.1:p.Pro492Ser
XM_017017331.2:c.1474C>T	XP_016872820.1:p.Pro492Ser
XM_017017332.2:c.1288C>T	XP_016872821.1:p.Pro430Ser
XM_017017333.2:c.1255C>T	XP_016872822.1:p.Pro419Ser
XM_017017334.2:c.1255C>T	XP_016872823.1:p.Pro419Ser
XM_017017335.2:c.1255C>T	XP_016872824.1:p.Pro419Ser
XM_017017336.2:c.1147C>T	XP_016872825.1:p.Pro383Ser
XM_024448392.1:c.1987C>T	XP_024304160.1:p.Pro663Ser
XM_024448393.1:c.1474C>T	XP_024304161.1:p.Pro492Ser
XR_001747789.2:n.2129C>T
XR_247191.3:n.2251C>T
NM_139075.4:c.2197C>T MANE Select	NP_620714.2:p.Pro733Ser