Canonical Allele Identifier: CA1638240712

Gene: SLC17A5

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.73644778_73644779delinsAT , CM000668.2:g.73644778_73644779delinsAT	GRCh38
NC_000006.11:g.74354501_74354502delinsAT , CM000668.1:g.74354501_74354502delinsAT	GRCh37
NC_000006.10:g.74411222_74411223delinsAT	NCBI36
NG_008272.1:g.14236_14237delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355773.6:c.95-176_95-175delinsAT MANE Select	ENSP00000348019.5:n.95-176_95-175delinsAT
ENST00000355773.5:c.95-176_95-175delinsAT	ENSP00000348019.5:n.95-176_95-175delinsAT
NM_012434.4:c.95-176_95-175delinsAT	NP_036566.1:n.95-176_95-175delinsAT
XM_005248710.2:c.44-176_44-175delinsAT	XP_005248767.1:n.44-176_44-175delinsAT
XM_005248711.1:c.-104-176_-104-175delinsAT	XP_005248768.1:n.-104-176_-104-175delinsAT
XM_011535750.1:c.95-176_95-175delinsAT	XP_011534052.1:n.95-176_95-175delinsAT
XM_011535751.1:c.95-176_95-175delinsAT	XP_011534053.1:n.95-176_95-175delinsAT
NM_012434.5:c.95-176_95-175delinsAT MANE Select	NP_036566.1:n.95-176_95-175delinsAT
NM_001382629.1:c.61-2855_61-2854delinsAT	NP_001369558.1:n.61-2855_61-2854delinsAT
NM_001382630.1:c.95-176_95-175delinsAT	NP_001369559.1:n.95-176_95-175delinsAT
NM_001382631.1:c.116-176_116-175delinsAT	NP_001369560.1:n.116-176_116-175delinsAT
NM_001382632.1:c.95-176_95-175delinsAT	NP_001369561.1:n.95-176_95-175delinsAT
NM_001382633.1:c.95-176_95-175delinsAT	NP_001369562.1:n.95-176_95-175delinsAT
NM_001382634.1:c.95-176_95-175delinsAT	NP_001369563.1:n.95-176_95-175delinsAT
NM_001382635.1:c.95-176_95-175delinsAT	NP_001369564.1:n.95-176_95-175delinsAT
NM_001382636.1:c.61-2855_61-2854delinsAT	NP_001369565.1:n.61-2855_61-2854delinsAT