Canonical Allele Identifier: CA2679404150

Gene: SLC17A5

Linked Data

• gnomAD v4: 6-73621783-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73621783C>T , CM000668.2:g.73621783C>T	GRCh38
NC_000006.11:g.74331506C>T , CM000668.1:g.74331506C>T	GRCh37
NC_000006.10:g.74388227C>T	NCBI36
NG_008272.1:g.37232G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000355773.6:c.978+21G>A MANE Select	ENSP00000348019.5:n.978+21G>A
ENST00000355773.5:c.978+21G>A	ENSP00000348019.5:n.978+21G>A
NM_012434.4:c.978+21G>A	NP_036566.1:n.978+21G>A
XM_005248710.2:c.927+21G>A	XP_005248767.1:n.927+21G>A
XM_005248711.1:c.780+21G>A	XP_005248768.1:n.780+21G>A
XM_011535750.1:c.978+21G>A	XP_011534052.1:n.978+21G>A
NM_012434.5:c.978+21G>A MANE Select	NP_036566.1:n.978+21G>A
NM_001382629.1:c.747+21G>A	NP_001369558.1:n.747+21G>A
NM_001382630.1:c.978+21G>A	NP_001369559.1:n.978+21G>A
NM_001382631.1:c.999+21G>A	NP_001369560.1:n.999+21G>A
NM_001382632.1:c.891+21G>A	NP_001369561.1:n.891+21G>A
NM_001382633.1:c.978+21G>A	NP_001369562.1:n.978+21G>A
NM_001382634.1:c.820-6336G>A	NP_001369563.1:n.820-6336G>A
NM_001382635.1:c.975+21G>A	NP_001369564.1:n.975+21G>A
NM_001382636.1:c.660+21G>A	NP_001369565.1:n.660+21G>A