Canonical Allele Identifier: CA364719465

Gene: SLC17A5

Linked Data

• dbSNP Id: rs1554164485
• MyVariant Identifiers: chr6:g.74354359_74354360insC (hg19) ; chr6:g.73644636_73644637insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73644636_73644637insC , CM000668.2:g.73644636_73644637insC	GRCh38
NC_000006.11:g.74354359_74354360insC , CM000668.1:g.74354359_74354360insC	GRCh37
NC_000006.10:g.74411080_74411081insC	NCBI36
NG_008272.1:g.14378_14379insG

Transcript Alleles

HGVS	Amino-acid change
ENST00000355773.6:c.95-34_95-33insG MANE Select	ENSP00000348019.5:n.95-34_95-33insG
ENST00000355773.5:c.95-34_95-33insG	ENSP00000348019.5:n.95-34_95-33insG
NM_012434.4:c.95-34_95-33insG	NP_036566.1:n.95-34_95-33insG
XM_005248710.2:c.44-34_44-33insG	XP_005248767.1:n.44-34_44-33insG
XM_005248711.1:c.-104-34_-104-33insG	XP_005248768.1:n.-104-34_-104-33insG
XM_011535750.1:c.95-34_95-33insG	XP_011534052.1:n.95-34_95-33insG
XM_011535751.1:c.95-34_95-33insG	XP_011534053.1:n.95-34_95-33insG
NM_012434.5:c.95-34_95-33insG MANE Select	NP_036566.1:n.95-34_95-33insG
NM_001382629.1:c.61-2713_61-2712insG	NP_001369558.1:n.61-2713_61-2712insG
NM_001382630.1:c.95-34_95-33insG	NP_001369559.1:n.95-34_95-33insG
NM_001382631.1:c.116-34_116-33insG	NP_001369560.1:n.116-34_116-33insG
NM_001382632.1:c.95-34_95-33insG	NP_001369561.1:n.95-34_95-33insG
NM_001382633.1:c.95-34_95-33insG	NP_001369562.1:n.95-34_95-33insG
NM_001382634.1:c.95-34_95-33insG	NP_001369563.1:n.95-34_95-33insG
NM_001382635.1:c.95-34_95-33insG	NP_001369564.1:n.95-34_95-33insG
NM_001382636.1:c.61-2713_61-2712insG	NP_001369565.1:n.61-2713_61-2712insG