Canonical Allele Identifier: CA15922870
Gene: TPGS2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.36791898C>T , CM000680.2:g.36791898C>T GRCh38
NC_000018.9:g.34371861C>T , CM000680.1:g.34371861C>T GRCh37
NC_000018.8:g.32625859C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000587129.5:c.657+6551G>A ENSP00000465551.1:n.657+6551G>A
ENST00000587382.5:c.621-1747G>A
ENST00000590258.2:c.137+6551G>A
ENST00000590652.5:c.226+6551G>A
ENST00000590842.5:c.658-4819G>A ENSP00000464780.1:n.658-4819G>A
ENST00000591906.5:c.527-4916G>A
ENST00000610723.4:c.383-4819G>A ENSP00000484407.1:n.383-4819G>A
ENST00000614939.4:c.657+6551G>A ENSP00000478553.1:n.657+6551G>A
NM_001271951.1:c.658-4819G>A NP_001258880.1:n.658-4819G>A
NM_001271953.1:c.658-4916G>A NP_001258882.1:n.658-4916G>A
NM_001271955.1:c.383-4819G>A NP_001258884.1:n.383-4819G>A
NM_001271956.1:c.657+6551G>A NP_001258885.1:n.657+6551G>A
XM_005258242.3:c.529-4819G>A XP_005258299.1:n.529-4819G>A
XM_011525912.1:c.763-4819G>A XP_011524214.1:n.763-4819G>A
XM_011525914.1:c.619-4819G>A XP_011524216.1:n.619-4819G>A
XM_011525915.1:c.762+6551G>A XP_011524217.1:n.762+6551G>A
XM_011525916.1:c.763-4916G>A XP_011524218.1:n.763-4916G>A
XM_011525917.1:c.514-4819G>A XP_011524219.1:n.514-4819G>A
XR_935214.1:n.1388+6551G>A
NM_001330572.1:c.657+6551G>A NP_001317501.1:n.657+6551G>A
XM_005258242.4:c.529-4819G>A XP_005258299.1:n.529-4819G>A
XM_011525917.3:c.514-4819G>A XP_011524219.1:n.514-4819G>A
XM_017025701.2:c.657+6551G>A XP_016881190.1:n.657+6551G>A
XM_017025702.2:c.528+6551G>A XP_016881191.1:n.528+6551G>A
XM_017025703.2:c.513+6551G>A XP_016881192.1:n.513+6551G>A
XR_001753180.2:n.892+6551G>A
XR_001753181.2:n.759+6551G>A
NM_001271953.2:c.658-4916G>A NP_001258882.1:n.658-4916G>A
NM_001330572.2:c.657+6551G>A NP_001317501.1:n.657+6551G>A
NM_001271951.2:c.658-4819G>A NP_001258880.1:n.658-4819G>A
NM_001271955.2:c.383-4819G>A NP_001258884.1:n.383-4819G>A
NM_001271956.2:c.657+6551G>A NP_001258885.1:n.657+6551G>A
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