Canonical Allele Identifier: CA1616755201
Gene: SLC17A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.25787547_25787548delinsTC , CM000668.2:g.25787547_25787548delinsTC GRCh38
NC_000006.11:g.25787775_25787776delinsTC , CM000668.1:g.25787775_25787776delinsTC GRCh37
NC_000006.10:g.25895754_25895755delinsTC NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000244527.10:c.*3-4330_*3-4329delinsGA MANE Select ENSP00000244527.4:n.*3-4330_*3-4329delins...
ENST00000244527.8:c.*3-4330_*3-4329delinsGA ENSP00000244527.4:n.*3-4330_*3-4329delins...
ENST00000377886.6:c.*658-4330_*658-4329delinsGA ENSP00000367118.2:n.*658-4330_*658-4329de...
NM_005074.3:c.*3-4330_*3-4329delinsGA NP_005065.2:n.*3-4330_*3-4329delinsGA
XM_011514818.1:c.1179-4330_1179-4329delinsGA XP_011513120.1:n.1179-4330_1179-4329delin...
XM_011514818.2:c.1329-4330_1329-4329delinsGA XP_011513120.2:n.1329-4330_1329-4329delin...
XM_017011200.1:c.*3-4330_*3-4329delinsGA XP_016866689.1:n.*3-4330_*3-4329delinsGA
XM_017011201.2:c.*2+11235_*2+11236delinsGA XP_016866690.1:n.*2+11235_*2+11236delinsG...
NM_005074.5:c.*3-4330_*3-4329delinsGA MANE Select NP_005065.2:n.*3-4330_*3-4329delinsGA