Canonical Allele Identifier: CA364720073

Gene: SLC17A5

Linked Data

• gnomAD v4: 6-73600424-A-G
• MyVariant Identifiers: chr6:g.74310147A>G (hg19) ; chr6:g.73600424A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73600424A>G , CM000668.2:g.73600424A>G	GRCh38
NC_000006.11:g.74310147A>G , CM000668.1:g.74310147A>G	GRCh37
NC_000006.10:g.74366868A>G	NCBI36
NG_008272.1:g.58591T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355773.6:c.1277T>C MANE Select	ENSP00000348019.5:p.Leu426Pro
ENST00000355773.5:c.1277T>C	ENSP00000348019.5:p.Leu426Pro
NM_012434.4:c.1277T>C	NP_036566.1:p.Leu426Pro
XM_005248710.2:c.1226T>C	XP_005248767.1:p.Leu409Pro
XM_005248711.1:c.1079T>C	XP_005248768.1:p.Leu360Pro
XM_011535750.1:c.1129T>C	XP_011534052.1:p.Trp377Arg
NM_012434.5:c.1277T>C MANE Select	NP_036566.1:p.Leu426Pro
NM_001382629.1:c.1046T>C	NP_001369558.1:p.Leu349Pro
NM_001382630.1:c.1260-5210T>C	NP_001369559.1:n.1260-5210T>C
NM_001382631.1:c.1298T>C	NP_001369560.1:p.Leu433Pro
NM_001382632.1:c.1190T>C	NP_001369561.1:p.Leu397Pro
NM_001382633.1:c.1277T>C	NP_001369562.1:p.Leu426Pro
NM_001382634.1:c.1118T>C	NP_001369563.1:p.Leu373Pro
NM_001382635.1:c.1274T>C	NP_001369564.1:p.Leu425Pro
NM_001382636.1:c.959T>C	NP_001369565.1:p.Leu320Pro