Canonical Allele Identifier: CA381652211

Gene: TPCN2

Linked Data

• dbSNP Id: rs1188693738
• MyVariant Identifiers: chr11:g.68855403C>G (hg19) ; chr11:g.69087935C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69087935C>G , CM000673.2:g.69087935C>G	GRCh38
NC_000011.9:g.68855403C>G , CM000673.1:g.68855403C>G	GRCh37
NC_000011.8:g.68611979C>G	NCBI36
NG_016153.1:g.44054C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000692585.1:c.1098C>G	ENSP00000509200.1:p.His366Gln
ENST00000294309.8:c.2241C>G MANE Select	ENSP00000294309.3:p.His747Gln
ENST00000635811.1:c.*436C>G	ENSP00000490341.1:n.*436C>G
ENST00000637084.1:c.1098C>G	ENSP00000490615.1:p.His366Gln
ENST00000637342.1:c.2003+2005C>G	ENSP00000490171.1:n.2003+2005C>G
ENST00000637504.1:c.*33+2649C>G	ENSP00000489759.1:n.*33+2649C>G
ENST00000294309.7:c.2241C>G	ENSP00000294309.3:p.His747Gln
ENST00000442692.2:n.1707C>G
ENST00000542467.1:c.1695C>G	ENSP00000445551.1:p.His565Gln
NM_139075.3:c.2241C>G	NP_620714.2:p.His747Gln
XM_005273824.2:c.2238C>G	XP_005273881.1:p.His746Gln
XM_005273826.2:c.1986C>G	XP_005273883.1:p.His662Gln
XM_005273830.2:c.1548C>G	XP_005273887.1:p.His516Gln
XM_005273831.2:c.1548C>G	XP_005273888.1:p.His516Gln
XM_005273832.2:c.1518C>G	XP_005273889.1:p.His506Gln
XM_006718453.2:c.1639+6436C>G	XP_006718516.1:n.1639+6436C>G
XM_006718454.2:c.1689+6436C>G	XP_006718517.1:n.1689+6436C>G
XM_011544802.1:c.2001C>G	XP_011543104.1:p.His667Gln
XM_011544807.1:c.1545C>G	XP_011543109.1:p.His515Gln
XM_011544808.1:c.1410C>G	XP_011543110.1:p.His470Gln
XM_005273824.4:c.2238C>G	XP_005273881.1:p.His746Gln
XM_005273826.4:c.1986C>G	XP_005273883.1:p.His662Gln
XM_005273830.4:c.1548C>G	XP_005273887.1:p.His516Gln
XM_005273831.4:c.1548C>G	XP_005273888.1:p.His516Gln
XM_005273832.4:c.1518C>G	XP_005273889.1:p.His506Gln
XM_011544802.3:c.2001C>G	XP_011543104.1:p.His667Gln
XM_011544807.3:c.1545C>G	XP_011543109.1:p.His515Gln
XM_011544808.3:c.1410C>G	XP_011543110.1:p.His470Gln
XM_017017328.2:c.2022C>G	XP_016872817.1:p.His674Gln
XM_017017329.2:c.2019C>G	XP_016872818.1:p.His673Gln
XM_017017330.2:c.1518C>G	XP_016872819.1:p.His506Gln
XM_017017331.2:c.1518C>G	XP_016872820.1:p.His506Gln
XM_017017332.2:c.1332C>G	XP_016872821.1:p.His444Gln
XM_017017333.2:c.1299C>G	XP_016872822.1:p.His433Gln
XM_017017334.2:c.1299C>G	XP_016872823.1:p.His433Gln
XM_017017335.2:c.1299C>G	XP_016872824.1:p.His433Gln
XM_017017336.2:c.1191C>G	XP_016872825.1:p.His397Gln
XM_024448392.1:c.2031C>G	XP_024304160.1:p.His677Gln
XM_024448393.1:c.1518C>G	XP_024304161.1:p.His506Gln
XR_001747789.2:n.2173C>G
XR_247191.3:n.2295C>G
NM_139075.4:c.2241C>G MANE Select	NP_620714.2:p.His747Gln