Canonical Allele Identifier: CA364713555

Gene: SLC17A5

Linked Data

• MyVariant Identifiers: chr6:g.74331612T>A (hg19) ; chr6:g.73621889T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73621889T>A , CM000668.2:g.73621889T>A	GRCh38
NC_000006.11:g.74331612T>A , CM000668.1:g.74331612T>A	GRCh37
NC_000006.10:g.74388333T>A	NCBI36
NG_008272.1:g.37126A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000355773.6:c.893A>T MANE Select	ENSP00000348019.5:p.His298Leu
ENST00000355773.5:c.893A>T	ENSP00000348019.5:p.His298Leu
NM_012434.4:c.893A>T	NP_036566.1:p.His298Leu
XM_005248710.2:c.842A>T	XP_005248767.1:p.His281Leu
XM_005248711.1:c.695A>T	XP_005248768.1:p.His232Leu
XM_011535750.1:c.893A>T	XP_011534052.1:p.His298Leu
NM_012434.5:c.893A>T MANE Select	NP_036566.1:p.His298Leu
NM_001382629.1:c.662A>T	NP_001369558.1:p.His221Leu
NM_001382630.1:c.893A>T	NP_001369559.1:p.His298Leu
NM_001382631.1:c.914A>T	NP_001369560.1:p.His305Leu
NM_001382632.1:c.806A>T	NP_001369561.1:p.His269Leu
NM_001382633.1:c.893A>T	NP_001369562.1:p.His298Leu
NM_001382634.1:c.820-6442A>T	NP_001369563.1:n.820-6442A>T
NM_001382635.1:c.890A>T	NP_001369564.1:p.His297Leu
NM_001382636.1:c.575A>T	NP_001369565.1:p.His192Leu