Canonical Allele Identifier: CA1638231827

Gene: SLC17A5

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73615425G= , CM000668.2:g.73615425G=	GRCh38
NC_000006.11:g.74325148G= , CM000668.1:g.74325148G=	GRCh37
NC_000006.10:g.74381869G=	NCBI36
NG_008272.1:g.43590C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355773.6:c.1001C= MANE Select	ENSP00000348019.5:p.Pro334=
ENST00000355773.5:c.1001C=	ENSP00000348019.5:p.Pro334=
NM_012434.4:c.1001C=	NP_036566.1:p.Pro334=
XM_005248710.2:c.950C=	XP_005248767.1:p.Pro317=
XM_005248711.1:c.803C=	XP_005248768.1:p.Pro268=
XM_011535750.1:c.1001C=	XP_011534052.1:p.Pro334=
NM_012434.5:c.1001C= MANE Select	NP_036566.1:p.Pro334=
NM_001382629.1:c.770C=	NP_001369558.1:p.Pro257=
NM_001382630.1:c.1001C=	NP_001369559.1:p.Pro334=
NM_001382631.1:c.1022C=	NP_001369560.1:p.Pro341=
NM_001382632.1:c.914C=	NP_001369561.1:p.Pro305=
NM_001382633.1:c.1001C=	NP_001369562.1:p.Pro334=
NM_001382634.1:c.842C=	NP_001369563.1:p.Pro281=
NM_001382635.1:c.998C=	NP_001369564.1:p.Pro333=
NM_001382636.1:c.683C=	NP_001369565.1:p.Pro228=