Canonical Allele Identifier: CA1638234800

Gene: SLC17A5

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73621901A= , CM000668.2:g.73621901A=	GRCh38
NC_000006.11:g.74331624A= , CM000668.1:g.74331624A=	GRCh37
NC_000006.10:g.74388345A=	NCBI36
NG_008272.1:g.37114T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000355773.6:c.881T= MANE Select	ENSP00000348019.5:p.Ile294=
ENST00000355773.5:c.881T=	ENSP00000348019.5:p.Ile294=
NM_012434.4:c.881T=	NP_036566.1:p.Ile294=
XM_005248710.2:c.830T=	XP_005248767.1:p.Ile277=
XM_005248711.1:c.683T=	XP_005248768.1:p.Ile228=
XM_011535750.1:c.881T=	XP_011534052.1:p.Ile294=
NM_012434.5:c.881T= MANE Select	NP_036566.1:p.Ile294=
NM_001382629.1:c.650T=	NP_001369558.1:p.Ile217=
NM_001382630.1:c.881T=	NP_001369559.1:p.Ile294=
NM_001382631.1:c.902T=	NP_001369560.1:p.Ile301=
NM_001382632.1:c.794T=	NP_001369561.1:p.Ile265=
NM_001382633.1:c.881T=	NP_001369562.1:p.Ile294=
NM_001382634.1:c.820-6454T=	NP_001369563.1:n.820-6454T=
NM_001382635.1:c.878T=	NP_001369564.1:p.Ile293=
NM_001382636.1:c.563T=	NP_001369565.1:p.Ile188=