Canonical Allele Identifier: CA2614769516

Gene: TPCN2

Linked Data

• gnomAD v4: 11-69087974-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69087974C>A , CM000673.2:g.69087974C>A	GRCh38
NC_000011.9:g.68855442C>A , CM000673.1:g.68855442C>A	GRCh37
NC_000011.8:g.68612018C>A	NCBI36
NG_016153.1:g.44093C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000692585.1:c.1137C>A	ENSP00000509200.1:n.1137C>A
ENST00000294309.8:c.*21C>A MANE Select	ENSP00000294309.3:n.*21C>A
ENST00000635811.1:c.*475C>A	ENSP00000490341.1:n.*475C>A
ENST00000637084.1:c.1137C>A	ENSP00000490615.1:n.1137C>A
ENST00000637342.1:c.2003+2044C>A	ENSP00000490171.1:n.2003+2044C>A
ENST00000637504.1:c.*33+2688C>A	ENSP00000489759.1:n.*33+2688C>A
ENST00000294309.7:c.*21C>A	ENSP00000294309.3:n.*21C>A
ENST00000442692.2:n.1746C>A
ENST00000542467.1:c.*21C>A	ENSP00000445551.1:n.*21C>A
NM_139075.3:c.*21C>A	NP_620714.2:n.*21C>A
XM_005273824.2:c.*21C>A	XP_005273881.1:n.*21C>A
XM_005273826.2:c.*21C>A	XP_005273883.1:n.*21C>A
XM_005273830.2:c.*21C>A	XP_005273887.1:n.*21C>A
XM_005273831.2:c.*21C>A	XP_005273888.1:n.*21C>A
XM_005273832.2:c.*21C>A	XP_005273889.1:n.*21C>A
XM_006718453.2:c.1639+6475C>A	XP_006718516.1:n.1639+6475C>A
XM_006718454.2:c.1689+6475C>A	XP_006718517.1:n.1689+6475C>A
XM_011544802.1:c.*21C>A	XP_011543104.1:n.*21C>A
XM_011544807.1:c.*21C>A	XP_011543109.1:n.*21C>A
XM_011544808.1:c.*21C>A	XP_011543110.1:n.*21C>A
XM_005273824.4:c.*21C>A	XP_005273881.1:n.*21C>A
XM_005273826.4:c.*21C>A	XP_005273883.1:n.*21C>A
XM_005273830.4:c.*21C>A	XP_005273887.1:n.*21C>A
XM_005273831.4:c.*21C>A	XP_005273888.1:n.*21C>A
XM_005273832.4:c.*21C>A	XP_005273889.1:n.*21C>A
XM_011544802.3:c.*21C>A	XP_011543104.1:n.*21C>A
XM_011544807.3:c.*21C>A	XP_011543109.1:n.*21C>A
XM_011544808.3:c.*21C>A	XP_011543110.1:n.*21C>A
XM_017017328.2:c.*21C>A	XP_016872817.1:n.*21C>A
XM_017017329.2:c.*21C>A	XP_016872818.1:n.*21C>A
XM_017017330.2:c.*21C>A	XP_016872819.1:n.*21C>A
XM_017017331.2:c.*21C>A	XP_016872820.1:n.*21C>A
XM_017017332.2:c.*21C>A	XP_016872821.1:n.*21C>A
XM_017017333.2:c.*21C>A	XP_016872822.1:n.*21C>A
XM_017017334.2:c.*21C>A	XP_016872823.1:n.*21C>A
XM_017017335.2:c.*21C>A	XP_016872824.1:n.*21C>A
XM_017017336.2:c.*21C>A	XP_016872825.1:n.*21C>A
XM_024448392.1:c.*21C>A	XP_024304160.1:n.*21C>A
XM_024448393.1:c.*21C>A	XP_024304161.1:n.*21C>A
XR_001747789.2:n.2212C>A
XR_247191.3:n.2334C>A
NM_139075.4:c.*21C>A MANE Select	NP_620714.2:n.*21C>A