Canonical Allele Identifier: CA1638223458

Gene: SLC17A5

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73642118_73642119delinsAC , CM000668.2:g.73642118_73642119delinsAC	GRCh38
NC_000006.11:g.74351841_74351842delinsAC , CM000668.1:g.74351841_74351842delinsAC	GRCh37
NC_000006.10:g.74408562_74408563delinsAC	NCBI36
NG_008272.1:g.16896_16897delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355773.6:c.292-195_292-194delinsGT MANE Select	ENSP00000348019.5:n.292-195_292-194delinsGT
ENST00000355773.5:c.292-195_292-194delinsGT	ENSP00000348019.5:n.292-195_292-194delinsGT
ENST00000481996.1:n.58-195_58-194delinsGT
NM_012434.4:c.292-195_292-194delinsGT	NP_036566.1:n.292-195_292-194delinsGT
XM_005248710.2:c.241-195_241-194delinsGT	XP_005248767.1:n.241-195_241-194delinsGT
XM_005248711.1:c.94-195_94-194delinsGT	XP_005248768.1:n.94-195_94-194delinsGT
XM_011535750.1:c.292-195_292-194delinsGT	XP_011534052.1:n.292-195_292-194delinsGT
XM_011535751.1:c.292-195_292-194delinsGT	XP_011534053.1:n.292-195_292-194delinsGT
NM_012434.5:c.292-195_292-194delinsGT MANE Select	NP_036566.1:n.292-195_292-194delinsGT
NM_001382629.1:c.61-195_61-194delinsGT	NP_001369558.1:n.61-195_61-194delinsGT
NM_001382630.1:c.292-195_292-194delinsGT	NP_001369559.1:n.292-195_292-194delinsGT
NM_001382631.1:c.313-195_313-194delinsGT	NP_001369560.1:n.313-195_313-194delinsGT
NM_001382632.1:c.292-195_292-194delinsGT	NP_001369561.1:n.292-195_292-194delinsGT
NM_001382633.1:c.292-195_292-194delinsGT	NP_001369562.1:n.292-195_292-194delinsGT
NM_001382634.1:c.292-195_292-194delinsGT	NP_001369563.1:n.292-195_292-194delinsGT
NM_001382635.1:c.292-195_292-194delinsGT	NP_001369564.1:n.292-195_292-194delinsGT
NM_001382636.1:c.61-195_61-194delinsGT	NP_001369565.1:n.61-195_61-194delinsGT