Canonical Allele Identifier: CA1638223870

Gene: SLC17A5

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73600381C= , CM000668.2:g.73600381C=	GRCh38
NC_000006.11:g.74310104C= , CM000668.1:g.74310104C=	GRCh37
NC_000006.10:g.74366825C=	NCBI36
NG_008272.1:g.58634G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355773.6:c.1320G= MANE Select	ENSP00000348019.5:p.Gly440=
ENST00000355773.5:c.1320G=	ENSP00000348019.5:p.Gly440=
NM_012434.4:c.1320G=	NP_036566.1:p.Gly440=
XM_005248710.2:c.1269G=	XP_005248767.1:p.Gly423=
XM_005248711.1:c.1122G=	XP_005248768.1:p.Gly374=
XM_011535750.1:c.1172G=	XP_011534052.1:p.Gly391=
NM_012434.5:c.1320G= MANE Select	NP_036566.1:p.Gly440=
NM_001382629.1:c.1089G=	NP_001369558.1:p.Gly363=
NM_001382630.1:c.1260-5167G=	NP_001369559.1:n.1260-5167G=
NM_001382631.1:c.1341G=	NP_001369560.1:p.Gly447=
NM_001382632.1:c.1233G=	NP_001369561.1:p.Gly411=
NM_001382633.1:c.1320G=	NP_001369562.1:p.Gly440=
NM_001382634.1:c.1161G=	NP_001369563.1:p.Gly387=
NM_001382635.1:c.1317G=	NP_001369564.1:p.Gly439=
NM_001382636.1:c.1002G=	NP_001369565.1:p.Gly334=