Canonical Allele Identifier: CA1638234792

Gene: SLC17A5

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73621883G= , CM000668.2:g.73621883G=	GRCh38
NC_000006.11:g.74331606G= , CM000668.1:g.74331606G=	GRCh37
NC_000006.10:g.74388327G=	NCBI36
NG_008272.1:g.37132C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000355773.6:c.899C= MANE Select	ENSP00000348019.5:p.Ser300=
ENST00000355773.5:c.899C=	ENSP00000348019.5:p.Ser300=
NM_012434.4:c.899C=	NP_036566.1:p.Ser300=
XM_005248710.2:c.848C=	XP_005248767.1:p.Ser283=
XM_005248711.1:c.701C=	XP_005248768.1:p.Ser234=
XM_011535750.1:c.899C=	XP_011534052.1:p.Ser300=
NM_012434.5:c.899C= MANE Select	NP_036566.1:p.Ser300=
NM_001382629.1:c.668C=	NP_001369558.1:p.Ser223=
NM_001382630.1:c.899C=	NP_001369559.1:p.Ser300=
NM_001382631.1:c.920C=	NP_001369560.1:p.Ser307=
NM_001382632.1:c.812C=	NP_001369561.1:p.Ser271=
NM_001382633.1:c.899C=	NP_001369562.1:p.Ser300=
NM_001382634.1:c.820-6436C=	NP_001369563.1:n.820-6436C=
NM_001382635.1:c.896C=	NP_001369564.1:p.Ser299=
NM_001382636.1:c.581C=	NP_001369565.1:p.Ser194=