Canonical Allele Identifier: CA1638224270

Gene: SLC17A5

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73600727C= , CM000668.2:g.73600727C=	GRCh38
NC_000006.11:g.74310450C= , CM000668.1:g.74310450C=	GRCh37
NC_000006.10:g.74367171C=	NCBI36
NG_008272.1:g.58288G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355773.6:c.1260-286G= MANE Select	ENSP00000348019.5:n.1260-286G=
ENST00000355773.5:c.1260-286G=	ENSP00000348019.5:n.1260-286G=
NM_012434.4:c.1260-286G=	NP_036566.1:n.1260-286G=
XM_005248710.2:c.1209-286G=	XP_005248767.1:n.1209-286G=
XM_005248711.1:c.1062-286G=	XP_005248768.1:n.1062-286G=
XM_011535750.1:c.1112-286G=	XP_011534052.1:n.1112-286G=
NM_012434.5:c.1260-286G= MANE Select	NP_036566.1:n.1260-286G=
NM_001382629.1:c.1029-286G=	NP_001369558.1:n.1029-286G=
NM_001382630.1:c.1260-5513G=	NP_001369559.1:n.1260-5513G=
NM_001382631.1:c.1281-286G=	NP_001369560.1:n.1281-286G=
NM_001382632.1:c.1173-286G=	NP_001369561.1:n.1173-286G=
NM_001382633.1:c.1260-286G=	NP_001369562.1:n.1260-286G=
NM_001382634.1:c.1101-286G=	NP_001369563.1:n.1101-286G=
NM_001382635.1:c.1257-286G=	NP_001369564.1:n.1257-286G=
NM_001382636.1:c.942-286G=	NP_001369565.1:n.942-286G=