Canonical Allele Identifier: CA364720078

Gene: SLC17A5

Linked Data

• MyVariant Identifiers: chr6:g.74310150A>G (hg19) ; chr6:g.73600427A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73600427A>G , CM000668.2:g.73600427A>G	GRCh38
NC_000006.11:g.74310150A>G , CM000668.1:g.74310150A>G	GRCh37
NC_000006.10:g.74366871A>G	NCBI36
NG_008272.1:g.58588T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355773.6:c.1274T>C MANE Select	ENSP00000348019.5:p.Leu425Pro
ENST00000355773.5:c.1274T>C	ENSP00000348019.5:p.Leu425Pro
NM_012434.4:c.1274T>C	NP_036566.1:p.Leu425Pro
XM_005248710.2:c.1223T>C	XP_005248767.1:p.Leu408Pro
XM_005248711.1:c.1076T>C	XP_005248768.1:p.Leu359Pro
XM_011535750.1:c.1126T>C	XP_011534052.1:p.Ser376Pro
NM_012434.5:c.1274T>C MANE Select	NP_036566.1:p.Leu425Pro
NM_001382629.1:c.1043T>C	NP_001369558.1:p.Leu348Pro
NM_001382630.1:c.1260-5213T>C	NP_001369559.1:n.1260-5213T>C
NM_001382631.1:c.1295T>C	NP_001369560.1:p.Leu432Pro
NM_001382632.1:c.1187T>C	NP_001369561.1:p.Leu396Pro
NM_001382633.1:c.1274T>C	NP_001369562.1:p.Leu425Pro
NM_001382634.1:c.1115T>C	NP_001369563.1:p.Leu372Pro
NM_001382635.1:c.1271T>C	NP_001369564.1:p.Leu424Pro
NM_001382636.1:c.956T>C	NP_001369565.1:p.Leu319Pro