Canonical Allele Identifier: CA2679403372

Gene: SLC17A5

Linked Data

• gnomAD v4: 6-73600505-C-CTT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73600506_73600507dup , CM000668.2:g.73600506_73600507dup	GRCh38
NC_000006.11:g.74310229_74310230dup , CM000668.1:g.74310229_74310230dup	GRCh37
NC_000006.10:g.74366950_74366951dup	NCBI36
NG_008272.1:g.58508_58509dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355773.6:c.1260-66_1260-65dup MANE Select	ENSP00000348019.5:n.1260-66_1260-65dup
ENST00000355773.5:c.1260-66_1260-65dup	ENSP00000348019.5:n.1260-66_1260-65dup
NM_012434.4:c.1260-66_1260-65dup	NP_036566.1:n.1260-66_1260-65dup
XM_005248710.2:c.1209-66_1209-65dup	XP_005248767.1:n.1209-66_1209-65dup
XM_005248711.1:c.1062-66_1062-65dup	XP_005248768.1:n.1062-66_1062-65dup
XM_011535750.1:c.1112-66_1112-65dup	XP_011534052.1:n.1112-66_1112-65dup
NM_012434.5:c.1260-66_1260-65dup MANE Select	NP_036566.1:n.1260-66_1260-65dup
NM_001382629.1:c.1029-66_1029-65dup	NP_001369558.1:n.1029-66_1029-65dup
NM_001382630.1:c.1260-5293_1260-5292dup	NP_001369559.1:n.1260-5293_1260-5292dup
NM_001382631.1:c.1281-66_1281-65dup	NP_001369560.1:n.1281-66_1281-65dup
NM_001382632.1:c.1173-66_1173-65dup	NP_001369561.1:n.1173-66_1173-65dup
NM_001382633.1:c.1260-66_1260-65dup	NP_001369562.1:n.1260-66_1260-65dup
NM_001382634.1:c.1101-66_1101-65dup	NP_001369563.1:n.1101-66_1101-65dup
NM_001382635.1:c.1257-66_1257-65dup	NP_001369564.1:n.1257-66_1257-65dup
NM_001382636.1:c.942-66_942-65dup	NP_001369565.1:n.942-66_942-65dup