Canonical Allele Identifier: CA1638223808
Gene: SLC17A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.73600358G= , CM000668.2:g.73600358G= GRCh38
NC_000006.11:g.74310081G= , CM000668.1:g.74310081G= GRCh37
NC_000006.10:g.74366802G= NCBI36
NG_008272.1:g.58657C=

Transcript Alleles

HGVS Amino-acid change
ENST00000355773.6:c.1343C= MANE Select ENSP00000348019.5:p.Thr448=
ENST00000355773.5:c.1343C= ENSP00000348019.5:p.Thr448=
NM_012434.4:c.1343C= NP_036566.1:p.Thr448=
XM_005248710.2:c.1292C= XP_005248767.1:p.Thr431=
XM_005248711.1:c.1145C= XP_005248768.1:p.Thr382=
XM_011535750.1:c.*1C= XP_011534052.1:n.*1C=
NM_012434.5:c.1343C= MANE Select NP_036566.1:p.Thr448=
NM_001382629.1:c.1112C= NP_001369558.1:p.Thr371=
NM_001382630.1:c.1260-5144C= NP_001369559.1:n.1260-5144C=
NM_001382631.1:c.1364C= NP_001369560.1:p.Thr455=
NM_001382632.1:c.1256C= NP_001369561.1:p.Thr419=
NM_001382633.1:c.1343C= NP_001369562.1:p.Thr448=
NM_001382634.1:c.1184C= NP_001369563.1:p.Thr395=
NM_001382635.1:c.1340C= NP_001369564.1:p.Thr447=
NM_001382636.1:c.1025C= NP_001369565.1:p.Thr342=