Canonical Allele Identifier: CA1616810521
Gene: SLC17A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.25918654G= , CM000668.2:g.25918654G= GRCh38
NC_000006.11:g.25918882G= , CM000668.1:g.25918882G= GRCh37
NC_000006.10:g.26026861G= NCBI36
NG_034000.1:g.17073C=

Transcript Alleles

HGVS Amino-acid change
ENST00000377850.8:c.563-81C= MANE Select ENSP00000367081.3:n.563-81C=
ENST00000265425.3:c.563-81C= ENSP00000265425.3:n.563-81C=
ENST00000360488.7:c.563-81C= ENSP00000353677.3:n.563-81C=
ENST00000377850.7:c.563-81C= ENSP00000367081.3:n.563-81C=
NM_001286123.1:c.563-81C= NP_001273052.1:n.563-81C=
NM_001286125.1:c.563-81C= NP_001273054.1:n.563-81C=
NM_005835.3:c.563-81C= NP_005826.1:n.563-81C=
XM_005248784.2:c.563-81C= XP_005248841.1:n.563-81C=
XM_006714949.2:c.563-81C= XP_006715012.1:n.563-81C=
XM_006714950.1:c.494-81C= XP_006715013.1:n.494-81C=
XM_006714951.1:c.563-81C= XP_006715014.1:n.563-81C=
XM_011514227.1:c.563-81C= XP_011512529.1:n.563-81C=
XM_006714949.3:c.563-81C= XP_006715012.1:n.563-81C=
XM_006714950.2:c.494-81C= XP_006715013.1:n.494-81C=
XM_017010159.1:c.494-81C= XP_016865648.1:n.494-81C=
XM_017010160.1:c.563-81C= XP_016865649.1:n.563-81C=
NM_001286123.3:c.563-81C= MANE Select NP_001273052.1:n.563-81C=
NM_001286125.2:c.563-81C= NP_001273054.1:n.563-81C=
NM_005835.4:c.563-81C= NP_005826.1:n.563-81C=