Canonical Allele Identifier: CA2003749695

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027724_119027725delinsCA , CM000673.2:g.119027724_119027725delinsCA	GRCh38
NC_000011.9:g.118898434_118898435delinsCA , CM000673.1:g.118898434_118898435delinsCA	GRCh37
NC_000011.8:g.118403644_118403645delinsCA	NCBI36
NG_013331.1:g.8181_8182delinsTG , LRG_187:g.8181_8182delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.758_759delinsTG
ENST00000697845.1:n.682_683delinsTG
ENST00000697846.1:n.758_759delinsTG
ENST00000697847.1:n.758_759delinsTG
ENST00000697848.1:n.758_759delinsTG
ENST00000697849.1:n.1797_1798delinsTG
ENST00000697850.1:n.758_759delinsTG
ENST00000697851.1:n.2118_2119delinsTG
ENST00000638186.1:n.832_833delinsTG
ENST00000638360.1:n.664_665delinsTG
ENST00000638925.1:n.765_766delinsTG
ENST00000650539.1:n.934_935delinsTG
ENST00000330775.9:c.529-1_529delinsTG
ENST00000357590.9:c.529-1_529delinsTG
ENST00000524428.5:n.850_851delinsTG
ENST00000525039.5:n.952_953delinsTG
ENST00000525102.5:n.1286_1287delinsTG
ENST00000525372.5:n.529_530delinsTG
ENST00000526275.5:n.1310_1311delinsTG
ENST00000526626.6:n.491_492delinsTG
ENST00000527992.5:n.756_757delinsTG
ENST00000529510.5:n.399+469_399+470delinsTG
ENST00000530407.5:n.678_679delinsTG
ENST00000532085.1:n.3139_3140delinsTG
ENST00000532888.6:n.824_825delinsTG
ENST00000538950.5:c.310-1_310delinsTG
ENST00000545985.5:c.529-1_529delinsTG
NM_001164277.1:c.528_529delinsTG , LRG_187t1:c.528_529delinsTG	NP_001157749.1:p.Cys176=
NM_001164278.1:c.528_529delinsTG	NP_001157750.1:p.Cys176=
NM_001164279.1:c.309_310delinsTG	NP_001157751.1:p.Cys103=
NM_001164280.1:c.528_529delinsTG	NP_001157752.1:p.Cys176=
NM_001467.5:c.528_529delinsTG	NP_001458.1:p.Cys176=
NM_001164278.2:c.528_529delinsTG	NP_001157750.1:p.Cys176=
NM_001164279.2:c.309_310delinsTG	NP_001157751.1:p.Cys103=
NM_001164280.2:c.528_529delinsTG	NP_001157752.1:p.Cys176=
NM_001467.6:c.528_529delinsTG	NP_001458.1:p.Cys176=
NM_001164277.2:c.528_529delinsTG MANE Select	NP_001157749.1:p.Cys176=