Canonical Allele Identifier: CA1638234761

Gene: SLC17A5

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73621789A= , CM000668.2:g.73621789A=	GRCh38
NC_000006.11:g.74331512A= , CM000668.1:g.74331512A=	GRCh37
NC_000006.10:g.74388233A=	NCBI36
NG_008272.1:g.37226T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000355773.6:c.978+15T= MANE Select	ENSP00000348019.5:n.978+15T=
ENST00000355773.5:c.978+15T=	ENSP00000348019.5:n.978+15T=
NM_012434.4:c.978+15T=	NP_036566.1:n.978+15T=
XM_005248710.2:c.927+15T=	XP_005248767.1:n.927+15T=
XM_005248711.1:c.780+15T=	XP_005248768.1:n.780+15T=
XM_011535750.1:c.978+15T=	XP_011534052.1:n.978+15T=
NM_012434.5:c.978+15T= MANE Select	NP_036566.1:n.978+15T=
NM_001382629.1:c.747+15T=	NP_001369558.1:n.747+15T=
NM_001382630.1:c.978+15T=	NP_001369559.1:n.978+15T=
NM_001382631.1:c.999+15T=	NP_001369560.1:n.999+15T=
NM_001382632.1:c.891+15T=	NP_001369561.1:n.891+15T=
NM_001382633.1:c.978+15T=	NP_001369562.1:n.978+15T=
NM_001382634.1:c.820-6342T=	NP_001369563.1:n.820-6342T=
NM_001382635.1:c.975+15T=	NP_001369564.1:n.975+15T=
NM_001382636.1:c.660+15T=	NP_001369565.1:n.660+15T=