Canonical Allele Identifier: CA1638223457

Gene: SLC17A5

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73642112A= , CM000668.2:g.73642112A=	GRCh38
NC_000006.11:g.74351835A= , CM000668.1:g.74351835A=	GRCh37
NC_000006.10:g.74408556A=	NCBI36
NG_008272.1:g.16903T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355773.6:c.292-188T= MANE Select	ENSP00000348019.5:n.292-188T=
ENST00000355773.5:c.292-188T=	ENSP00000348019.5:n.292-188T=
ENST00000481996.1:n.58-188T=
NM_012434.4:c.292-188T=	NP_036566.1:n.292-188T=
XM_005248710.2:c.241-188T=	XP_005248767.1:n.241-188T=
XM_005248711.1:c.94-188T=	XP_005248768.1:n.94-188T=
XM_011535750.1:c.292-188T=	XP_011534052.1:n.292-188T=
XM_011535751.1:c.292-188T=	XP_011534053.1:n.292-188T=
NM_012434.5:c.292-188T= MANE Select	NP_036566.1:n.292-188T=
NM_001382629.1:c.61-188T=	NP_001369558.1:n.61-188T=
NM_001382630.1:c.292-188T=	NP_001369559.1:n.292-188T=
NM_001382631.1:c.313-188T=	NP_001369560.1:n.313-188T=
NM_001382632.1:c.292-188T=	NP_001369561.1:n.292-188T=
NM_001382633.1:c.292-188T=	NP_001369562.1:n.292-188T=
NM_001382634.1:c.292-188T=	NP_001369563.1:n.292-188T=
NM_001382635.1:c.292-188T=	NP_001369564.1:n.292-188T=
NM_001382636.1:c.61-188T=	NP_001369565.1:n.61-188T=