Canonical Allele Identifier: CA1638223689
Gene: SLC17A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.73600252G= , CM000668.2:g.73600252G= GRCh38
NC_000006.11:g.74309975G= , CM000668.1:g.74309975G= GRCh37
NC_000006.10:g.74366696G= NCBI36
NG_008272.1:g.58763C=

Transcript Alleles

HGVS Amino-acid change
ENST00000355773.6:c.1350+99C= MANE Select ENSP00000348019.5:n.1350+99C=
ENST00000355773.5:c.1350+99C= ENSP00000348019.5:n.1350+99C=
NM_012434.4:c.1350+99C= NP_036566.1:n.1350+99C=
XM_005248710.2:c.1299+99C= XP_005248767.1:n.1299+99C=
XM_005248711.1:c.1152+99C= XP_005248768.1:n.1152+99C=
XM_011535750.1:c.*8+99C= XP_011534052.1:n.*8+99C=
NM_012434.5:c.1350+99C= MANE Select NP_036566.1:n.1350+99C=
NM_001382629.1:c.1119+99C= NP_001369558.1:n.1119+99C=
NM_001382630.1:c.1260-5038C= NP_001369559.1:n.1260-5038C=
NM_001382631.1:c.1371+99C= NP_001369560.1:n.1371+99C=
NM_001382632.1:c.1263+99C= NP_001369561.1:n.1263+99C=
NM_001382633.1:c.1350+99C= NP_001369562.1:n.1350+99C=
NM_001382634.1:c.1191+99C= NP_001369563.1:n.1191+99C=
NM_001382635.1:c.1347+99C= NP_001369564.1:n.1347+99C=
NM_001382636.1:c.1032+99C= NP_001369565.1:n.1032+99C=