Canonical Allele Identifier: CA2679403289

Gene: SLC17A5

Linked Data

• gnomAD v4: 6-73600277-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73600281del , CM000668.2:g.73600281del	GRCh38
NC_000006.11:g.74310004del , CM000668.1:g.74310004del	GRCh37
NC_000006.10:g.74366725del	NCBI36
NG_008272.1:g.58737del

Transcript Alleles

HGVS	Amino-acid change
ENST00000355773.6:c.1350+73del MANE Select	ENSP00000348019.5:n.1350+73del
ENST00000355773.5:c.1350+73del	ENSP00000348019.5:n.1350+73del
NM_012434.4:c.1350+73del	NP_036566.1:n.1350+73del
XM_005248710.2:c.1299+73del	XP_005248767.1:n.1299+73del
XM_005248711.1:c.1152+73del	XP_005248768.1:n.1152+73del
XM_011535750.1:c.*8+73del	XP_011534052.1:n.*8+73del
NM_012434.5:c.1350+73del MANE Select	NP_036566.1:n.1350+73del
NM_001382629.1:c.1119+73del	NP_001369558.1:n.1119+73del
NM_001382630.1:c.1260-5064del	NP_001369559.1:n.1260-5064del
NM_001382631.1:c.1371+73del	NP_001369560.1:n.1371+73del
NM_001382632.1:c.1263+73del	NP_001369561.1:n.1263+73del
NM_001382633.1:c.1350+73del	NP_001369562.1:n.1350+73del
NM_001382634.1:c.1191+73del	NP_001369563.1:n.1191+73del
NM_001382635.1:c.1347+73del	NP_001369564.1:n.1347+73del
NM_001382636.1:c.1032+73del	NP_001369565.1:n.1032+73del