Canonical Allele Identifier: CA1638223802
Gene: SLC17A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.73600353C= , CM000668.2:g.73600353C= GRCh38
NC_000006.11:g.74310076C= , CM000668.1:g.74310076C= GRCh37
NC_000006.10:g.74366797C= NCBI36
NG_008272.1:g.58662G=

Transcript Alleles

HGVS Amino-acid change
ENST00000355773.6:c.1348G= MANE Select ENSP00000348019.5:p.Asp450=
ENST00000355773.5:c.1348G= ENSP00000348019.5:p.Asp450=
NM_012434.4:c.1348G= NP_036566.1:p.Asp450=
XM_005248710.2:c.1297G= XP_005248767.1:p.Asp433=
XM_005248711.1:c.1150G= XP_005248768.1:p.Asp384=
XM_011535750.1:c.*6G= XP_011534052.1:n.*6G=
NM_012434.5:c.1348G= MANE Select NP_036566.1:p.Asp450=
NM_001382629.1:c.1117G= NP_001369558.1:p.Asp373=
NM_001382630.1:c.1260-5139G= NP_001369559.1:n.1260-5139G=
NM_001382631.1:c.1369G= NP_001369560.1:p.Asp457=
NM_001382632.1:c.1261G= NP_001369561.1:p.Asp421=
NM_001382633.1:c.1348G= NP_001369562.1:p.Asp450=
NM_001382634.1:c.1189G= NP_001369563.1:p.Asp397=
NM_001382635.1:c.1345G= NP_001369564.1:p.Asp449=
NM_001382636.1:c.1030G= NP_001369565.1:p.Asp344=