Canonical Allele Identifier: CA381656329

Gene: TPCN2

Linked Data

• MyVariant Identifiers: chr11:g.68846421T>A (hg19) ; chr11:g.69078953T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69078953T>A , CM000673.2:g.69078953T>A	GRCh38
NC_000011.9:g.68846421T>A , CM000673.1:g.68846421T>A	GRCh37
NC_000011.8:g.68602997T>A	NCBI36
NG_016153.1:g.35072T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000692585.1:c.329T>A	ENSP00000509200.1:p.Leu110Gln
ENST00000294309.8:c.1472T>A MANE Select	ENSP00000294309.3:p.Leu491Gln
ENST00000635811.1:c.1472T>A	ENSP00000490341.1:p.Leu491Gln
ENST00000637084.1:c.329T>A	ENSP00000490615.1:p.Leu110Gln
ENST00000637342.1:c.1472T>A	ENSP00000490171.1:p.Leu491Gln
ENST00000637504.1:c.1472T>A	ENSP00000489759.1:p.Leu491Gln
ENST00000294309.7:c.1472T>A	ENSP00000294309.3:p.Leu491Gln
ENST00000442692.2:n.1065T>A
ENST00000535009.5:n.1281T>A
ENST00000542467.1:c.1472T>A	ENSP00000445551.1:p.Leu491Gln
NM_139075.3:c.1472T>A	NP_620714.2:p.Leu491Gln
XM_005273824.2:c.1469T>A	XP_005273881.1:p.Leu490Gln
XM_005273826.2:c.1217T>A	XP_005273883.1:p.Leu406Gln
XM_005273827.2:c.1472T>A	XP_005273884.1:p.Leu491Gln
XM_005273828.2:c.1472T>A	XP_005273885.1:p.Leu491Gln
XM_005273830.2:c.779T>A	XP_005273887.1:p.Leu260Gln
XM_005273831.2:c.779T>A	XP_005273888.1:p.Leu260Gln
XM_005273832.2:c.749T>A	XP_005273889.1:p.Leu250Gln
XM_006718453.2:c.1472T>A	XP_006718516.1:p.Leu491Gln
XM_006718454.2:c.1472T>A	XP_006718517.1:p.Leu491Gln
XM_006718456.2:c.1472T>A	XP_006718519.1:p.Leu491Gln
XM_011544802.1:c.1232T>A	XP_011543104.1:p.Leu411Gln
XM_011544803.1:c.1472T>A	XP_011543105.1:p.Leu491Gln
XM_011544804.1:c.1472T>A	XP_011543106.1:p.Leu491Gln
XM_011544805.1:c.1472T>A	XP_011543107.1:p.Leu491Gln
XM_011544806.1:c.1472T>A	XP_011543108.1:p.Leu491Gln
XM_011544807.1:c.776T>A	XP_011543109.1:p.Leu259Gln
XM_011544808.1:c.641T>A	XP_011543110.1:p.Leu214Gln
XR_247191.1:n.1573T>A
XM_005273824.4:c.1469T>A	XP_005273881.1:p.Leu490Gln
XM_005273826.4:c.1217T>A	XP_005273883.1:p.Leu406Gln
XM_005273830.4:c.779T>A	XP_005273887.1:p.Leu260Gln
XM_005273831.4:c.779T>A	XP_005273888.1:p.Leu260Gln
XM_005273832.4:c.749T>A	XP_005273889.1:p.Leu250Gln
XM_011544802.3:c.1232T>A	XP_011543104.1:p.Leu411Gln
XM_011544807.3:c.776T>A	XP_011543109.1:p.Leu259Gln
XM_011544808.3:c.641T>A	XP_011543110.1:p.Leu214Gln
XM_017017328.2:c.1303T>A	XP_016872817.1:p.Trp435Arg
XM_017017329.2:c.1300T>A	XP_016872818.1:p.Trp434Arg
XM_017017330.2:c.749T>A	XP_016872819.1:p.Leu250Gln
XM_017017331.2:c.749T>A	XP_016872820.1:p.Leu250Gln
XM_017017332.2:c.563T>A	XP_016872821.1:p.Leu188Gln
XM_017017333.2:c.580T>A	XP_016872822.1:p.Trp194Arg
XM_017017334.2:c.580T>A	XP_016872823.1:p.Trp194Arg
XM_017017335.2:c.580T>A	XP_016872824.1:p.Trp194Arg
XM_017017336.2:c.472T>A	XP_016872825.1:p.Trp158Arg
XM_024448392.1:c.1262T>A	XP_024304160.1:p.Leu421Gln
XM_024448393.1:c.749T>A	XP_024304161.1:p.Leu250Gln
XR_001747789.2:n.1404T>A
XR_001747790.2:n.1404T>A
XR_247191.3:n.1576T>A
NM_139075.4:c.1472T>A MANE Select	NP_620714.2:p.Leu491Gln