Canonical Allele Identifier: CA381652090

Gene: TPCN2

Linked Data

• MyVariant Identifiers: chr11:g.68855347A>G (hg19) ; chr11:g.69087879A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69087879A>G , CM000673.2:g.69087879A>G	GRCh38
NC_000011.9:g.68855347A>G , CM000673.1:g.68855347A>G	GRCh37
NC_000011.8:g.68611923A>G	NCBI36
NG_016153.1:g.43998A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000692585.1:c.1042A>G	ENSP00000509200.1:p.Ile348Val
ENST00000294309.8:c.2185A>G MANE Select	ENSP00000294309.3:p.Ile729Val
ENST00000635811.1:c.*380A>G	ENSP00000490341.1:n.*380A>G
ENST00000637084.1:c.1042A>G	ENSP00000490615.1:p.Ile348Val
ENST00000637342.1:c.2003+1949A>G	ENSP00000490171.1:n.2003+1949A>G
ENST00000637504.1:c.*33+2593A>G	ENSP00000489759.1:n.*33+2593A>G
ENST00000294309.7:c.2185A>G	ENSP00000294309.3:p.Ile729Val
ENST00000442692.2:n.1651A>G
ENST00000542467.1:c.1639A>G	ENSP00000445551.1:p.Ile547Val
NM_139075.3:c.2185A>G	NP_620714.2:p.Ile729Val
XM_005273824.2:c.2182A>G	XP_005273881.1:p.Ile728Val
XM_005273826.2:c.1930A>G	XP_005273883.1:p.Ile644Val
XM_005273830.2:c.1492A>G	XP_005273887.1:p.Ile498Val
XM_005273831.2:c.1492A>G	XP_005273888.1:p.Ile498Val
XM_005273832.2:c.1462A>G	XP_005273889.1:p.Ile488Val
XM_006718453.2:c.1639+6380A>G	XP_006718516.1:n.1639+6380A>G
XM_006718454.2:c.1689+6380A>G	XP_006718517.1:n.1689+6380A>G
XM_011544802.1:c.1945A>G	XP_011543104.1:p.Ile649Val
XM_011544807.1:c.1489A>G	XP_011543109.1:p.Ile497Val
XM_011544808.1:c.1354A>G	XP_011543110.1:p.Ile452Val
XR_247191.1:n.2236A>G
XM_005273824.4:c.2182A>G	XP_005273881.1:p.Ile728Val
XM_005273826.4:c.1930A>G	XP_005273883.1:p.Ile644Val
XM_005273830.4:c.1492A>G	XP_005273887.1:p.Ile498Val
XM_005273831.4:c.1492A>G	XP_005273888.1:p.Ile498Val
XM_005273832.4:c.1462A>G	XP_005273889.1:p.Ile488Val
XM_011544802.3:c.1945A>G	XP_011543104.1:p.Ile649Val
XM_011544807.3:c.1489A>G	XP_011543109.1:p.Ile497Val
XM_011544808.3:c.1354A>G	XP_011543110.1:p.Ile452Val
XM_017017328.2:c.1966A>G	XP_016872817.1:p.Ile656Val
XM_017017329.2:c.1963A>G	XP_016872818.1:p.Ile655Val
XM_017017330.2:c.1462A>G	XP_016872819.1:p.Ile488Val
XM_017017331.2:c.1462A>G	XP_016872820.1:p.Ile488Val
XM_017017332.2:c.1276A>G	XP_016872821.1:p.Ile426Val
XM_017017333.2:c.1243A>G	XP_016872822.1:p.Ile415Val
XM_017017334.2:c.1243A>G	XP_016872823.1:p.Ile415Val
XM_017017335.2:c.1243A>G	XP_016872824.1:p.Ile415Val
XM_017017336.2:c.1135A>G	XP_016872825.1:p.Ile379Val
XM_024448392.1:c.1975A>G	XP_024304160.1:p.Ile659Val
XM_024448393.1:c.1462A>G	XP_024304161.1:p.Ile488Val
XR_001747789.2:n.2117A>G
XR_247191.3:n.2239A>G
NM_139075.4:c.2185A>G MANE Select	NP_620714.2:p.Ile729Val