Canonical Allele Identifier: CA363169109
Gene: SLC17A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.25918535C>A , CM000668.2:g.25918535C>A GRCh38
NC_000006.11:g.25918763C>A , CM000668.1:g.25918763C>A GRCh37
NC_000006.10:g.26026742C>A NCBI36
NG_034000.1:g.17192G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000377850.8:c.601G>T MANE Select ENSP00000367081.3:p.Gly201Ter
ENST00000265425.3:c.601G>T ENSP00000265425.3:p.Gly201Ter
ENST00000360488.7:c.601G>T ENSP00000353677.3:p.Gly201Ter
ENST00000377850.7:c.601G>T ENSP00000367081.3:p.Gly201Ter
NM_001286123.1:c.601G>T NP_001273052.1:p.Gly201Ter
NM_001286125.1:c.601G>T NP_001273054.1:p.Gly201Ter
NM_005835.3:c.601G>T NP_005826.1:p.Gly201Ter
XM_005248784.2:c.601G>T XP_005248841.1:p.Gly201Ter
XM_006714949.2:c.601G>T XP_006715012.1:p.Gly201Ter
XM_006714950.1:c.532G>T XP_006715013.1:p.Gly178Ter
XM_006714951.1:c.601G>T XP_006715014.1:p.Gly201Ter
XM_011514227.1:c.601G>T XP_011512529.1:p.Gly201Ter
XM_006714949.3:c.601G>T XP_006715012.1:p.Gly201Ter
XM_006714950.2:c.532G>T XP_006715013.1:p.Gly178Ter
XM_017010159.1:c.532G>T XP_016865648.1:p.Gly178Ter
XM_017010160.1:c.601G>T XP_016865649.1:p.Gly201Ter
NM_001286123.3:c.601G>T MANE Select NP_001273052.1:p.Gly201Ter
NM_001286125.2:c.601G>T NP_001273054.1:p.Gly201Ter
NM_005835.4:c.601G>T NP_005826.1:p.Gly201Ter