Canonical Allele Identifier: CA2679405062

Gene: SLC17A5

Linked Data

• gnomAD v4: 6-73644424-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73644428del , CM000668.2:g.73644428del	GRCh38
NC_000006.11:g.74354151del , CM000668.1:g.74354151del	GRCh37
NC_000006.10:g.74410872del	NCBI36
NG_008272.1:g.14590del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355773.6:c.273del MANE Select	ENSP00000348019.5:p.Val92PhefsTer?
ENST00000355773.5:c.273del	ENSP00000348019.5:p.Val92PhefsTer?
ENST00000481996.1:n.39del
NM_012434.4:c.273del	NP_036566.1:p.Val92PhefsTer?
XM_005248710.2:c.222del	XP_005248767.1:p.Val75PhefsTer?
XM_005248711.1:c.75del	XP_005248768.1:p.Val26PhefsTer?
XM_011535750.1:c.273del	XP_011534052.1:p.Val92PhefsTer?
XM_011535751.1:c.273del	XP_011534053.1:p.Val92PhefsTer?
NM_012434.5:c.273del MANE Select	NP_036566.1:p.Val92PhefsTer?
NM_001382629.1:c.61-2501del	NP_001369558.1:n.61-2501del
NM_001382630.1:c.273del	NP_001369559.1:p.Val92PhefsTer?
NM_001382631.1:c.294del	NP_001369560.1:p.Val99PhefsTer?
NM_001382632.1:c.273del	NP_001369561.1:p.Val92PhefsTer?
NM_001382633.1:c.273del	NP_001369562.1:p.Val92PhefsTer?
NM_001382634.1:c.273del	NP_001369563.1:p.Val92PhefsTer?
NM_001382635.1:c.273del	NP_001369564.1:p.Val92PhefsTer?
NM_001382636.1:c.61-2501del	NP_001369565.1:n.61-2501del