Canonical Allele Identifier: CA381655979

Gene: TPCN2

Linked Data

• MyVariant Identifiers: chr11:g.68846255C>G (hg19) ; chr11:g.69078787C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69078787C>G , CM000673.2:g.69078787C>G	GRCh38
NC_000011.9:g.68846255C>G , CM000673.1:g.68846255C>G	GRCh37
NC_000011.8:g.68602831C>G	NCBI36
NG_016153.1:g.34906C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000692585.1:c.261C>G	ENSP00000509200.1:p.Ile87Met
ENST00000294309.8:c.1404C>G MANE Select	ENSP00000294309.3:p.Ile468Met
ENST00000635811.1:c.1404C>G	ENSP00000490341.1:p.Ile468Met
ENST00000637084.1:c.261C>G	ENSP00000490615.1:p.Ile87Met
ENST00000637342.1:c.1404C>G	ENSP00000490171.1:p.Ile468Met
ENST00000637504.1:c.1404C>G	ENSP00000489759.1:p.Ile468Met
ENST00000294309.7:c.1404C>G	ENSP00000294309.3:p.Ile468Met
ENST00000442692.2:n.997C>G
ENST00000535009.5:n.1213C>G
ENST00000542467.1:c.1404C>G	ENSP00000445551.1:p.Ile468Met
NM_139075.3:c.1404C>G	NP_620714.2:p.Ile468Met
XM_005273824.2:c.1401C>G	XP_005273881.1:p.Ile467Met
XM_005273826.2:c.1149C>G	XP_005273883.1:p.Ile383Met
XM_005273827.2:c.1404C>G	XP_005273884.1:p.Ile468Met
XM_005273828.2:c.1404C>G	XP_005273885.1:p.Ile468Met
XM_005273830.2:c.711C>G	XP_005273887.1:p.Ile237Met
XM_005273831.2:c.711C>G	XP_005273888.1:p.Ile237Met
XM_005273832.2:c.681C>G	XP_005273889.1:p.Ile227Met
XM_006718453.2:c.1404C>G	XP_006718516.1:p.Ile468Met
XM_006718454.2:c.1404C>G	XP_006718517.1:p.Ile468Met
XM_006718456.2:c.1404C>G	XP_006718519.1:p.Ile468Met
XM_011544802.1:c.1164C>G	XP_011543104.1:p.Ile388Met
XM_011544803.1:c.1404C>G	XP_011543105.1:p.Ile468Met
XM_011544804.1:c.1404C>G	XP_011543106.1:p.Ile468Met
XM_011544805.1:c.1404C>G	XP_011543107.1:p.Ile468Met
XM_011544806.1:c.1404C>G	XP_011543108.1:p.Ile468Met
XM_011544807.1:c.708C>G	XP_011543109.1:p.Ile236Met
XM_011544808.1:c.573C>G	XP_011543110.1:p.Ile191Met
XR_247191.1:n.1505C>G
XM_005273824.4:c.1401C>G	XP_005273881.1:p.Ile467Met
XM_005273826.4:c.1149C>G	XP_005273883.1:p.Ile383Met
XM_005273830.4:c.711C>G	XP_005273887.1:p.Ile237Met
XM_005273831.4:c.711C>G	XP_005273888.1:p.Ile237Met
XM_005273832.4:c.681C>G	XP_005273889.1:p.Ile227Met
XM_011544802.3:c.1164C>G	XP_011543104.1:p.Ile388Met
XM_011544807.3:c.708C>G	XP_011543109.1:p.Ile236Met
XM_011544808.3:c.573C>G	XP_011543110.1:p.Ile191Met
XM_017017328.2:c.1235C>G	XP_016872817.1:p.Ser412Cys
XM_017017329.2:c.1232C>G	XP_016872818.1:p.Ser411Cys
XM_017017330.2:c.681C>G	XP_016872819.1:p.Ile227Met
XM_017017331.2:c.681C>G	XP_016872820.1:p.Ile227Met
XM_017017332.2:c.495C>G	XP_016872821.1:p.Ile165Met
XM_017017333.2:c.512C>G	XP_016872822.1:p.Ser171Cys
XM_017017334.2:c.512C>G	XP_016872823.1:p.Ser171Cys
XM_017017335.2:c.512C>G	XP_016872824.1:p.Ser171Cys
XM_017017336.2:c.404C>G	XP_016872825.1:p.Ser135Cys
XM_024448392.1:c.1194C>G	XP_024304160.1:p.Ile398Met
XM_024448393.1:c.681C>G	XP_024304161.1:p.Ile227Met
XR_001747789.2:n.1336C>G
XR_001747790.2:n.1336C>G
XR_247191.3:n.1508C>G
NM_139075.4:c.1404C>G MANE Select	NP_620714.2:p.Ile468Met