Canonical Allele Identifier: CA364718827

Gene: SLC17A5

Linked Data

• gnomAD v4: 6-73644462-G-A
• MyVariant Identifiers: chr6:g.74354185G>A (hg19) ; chr6:g.73644462G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73644462G>A , CM000668.2:g.73644462G>A	GRCh38
NC_000006.11:g.74354185G>A , CM000668.1:g.74354185G>A	GRCh37
NC_000006.10:g.74410906G>A	NCBI36
NG_008272.1:g.14553C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355773.6:c.236C>T MANE Select	ENSP00000348019.5:p.Thr79Ile
ENST00000355773.5:c.236C>T	ENSP00000348019.5:p.Thr79Ile
ENST00000481996.1:n.2C>T
NM_012434.4:c.236C>T	NP_036566.1:p.Thr79Ile
XM_005248710.2:c.185C>T	XP_005248767.1:p.Thr62Ile
XM_005248711.1:c.38C>T	XP_005248768.1:p.Thr13Ile
XM_011535750.1:c.236C>T	XP_011534052.1:p.Thr79Ile
XM_011535751.1:c.236C>T	XP_011534053.1:p.Thr79Ile
NM_012434.5:c.236C>T MANE Select	NP_036566.1:p.Thr79Ile
NM_001382629.1:c.61-2538C>T	NP_001369558.1:n.61-2538C>T
NM_001382630.1:c.236C>T	NP_001369559.1:p.Thr79Ile
NM_001382631.1:c.257C>T	NP_001369560.1:p.Thr86Ile
NM_001382632.1:c.236C>T	NP_001369561.1:p.Thr79Ile
NM_001382633.1:c.236C>T	NP_001369562.1:p.Thr79Ile
NM_001382634.1:c.236C>T	NP_001369563.1:p.Thr79Ile
NM_001382635.1:c.236C>T	NP_001369564.1:p.Thr79Ile
NM_001382636.1:c.61-2538C>T	NP_001369565.1:n.61-2538C>T