Canonical Allele Identifier: CA2616334876

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119026733-A-AGGGTATGGGTGGTT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026737_119026738insATGGGTGGTTGGGT , CM000673.2:g.119026737_119026738insATGGGTGGTTGGGT	GRCh38
NC_000011.9:g.118897447_118897448insATGGGTGGTTGGGT , CM000673.1:g.118897447_118897448insATGGGTGGTTGGGT	GRCh37
NC_000011.8:g.118402657_118402658insATGGGTGGTTGGGT	NCBI36
NG_013331.1:g.9172_9173insAACCACCCATACCC , LRG_187:g.9172_9173insAACCACCCATACCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1014+203_1014+204insAACCACCCATACCC
ENST00000697845.1:n.1141_1142insAACCACCCATACCC
ENST00000697846.1:n.1014+203_1014+204insAACCACCCATACCC
ENST00000697847.1:n.1015-46_1015-45insAACCACCCATACCC
ENST00000697848.1:n.1015-46_1015-45insAACCACCCATACCC
ENST00000697849.1:n.2256_2257insAACCACCCATACCC
ENST00000697850.1:n.1015-46_1015-45insAACCACCCATACCC
ENST00000697851.1:n.2577_2578insAACCACCCATACCC
ENST00000638186.1:n.1089-46_1089-45insAACCACCCATACCC
ENST00000638360.1:n.921-46_921-45insAACCACCCATACCC
ENST00000638925.1:n.1022-46_1022-45insAACCACCCATACCC
ENST00000650539.1:n.1191-46_1191-45insAACCACCCATACCC
ENST00000330775.9:c.785-46_785-45insAACCACCCATACCC	ENSP00000476242.2:n.785-46_785-45insAACCACCCATACCC
ENST00000357590.9:c.785-46_785-45insAACCACCCATACCC	ENSP00000476176.2:n.785-46_785-45insAACCACCCATACCC
ENST00000524428.5:n.1106+203_1106+204insAACCACCCATACCC
ENST00000525039.5:n.1209-46_1209-45insAACCACCCATACCC
ENST00000525102.5:n.1543-46_1543-45insAACCACCCATACCC
ENST00000525372.5:n.786-46_786-45insAACCACCCATACCC
ENST00000526275.5:n.1567-46_1567-45insAACCACCCATACCC
ENST00000527992.5:n.1013-46_1013-45insAACCACCCATACCC
ENST00000529510.5:n.558+203_558+204insAACCACCCATACCC
ENST00000530407.5:n.935-46_935-45insAACCACCCATACCC
ENST00000532085.1:n.3598_3599insAACCACCCATACCC
ENST00000532888.6:n.1283_1284insAACCACCCATACCC
ENST00000538950.5:c.566-46_566-45insAACCACCCATACCC	ENSP00000475991.2:n.566-46_566-45insAACCACCCATACCC
ENST00000545985.5:c.785-46_785-45insAACCACCCATACCC	ENSP00000475241.2:n.785-46_785-45insAACCACCCATACCC
NM_001164277.1:c.785-46_785-45insAACCACCCATACCC , LRG_187t1:c.785-46_785-45insAACCACCCATACCC	NP_001157749.1:n.785-46_785-45insAACCACCCATACCC
NM_001164278.1:c.785-46_785-45insAACCACCCATACCC	NP_001157750.1:n.785-46_785-45insAACCACCCATACCC
NM_001164279.1:c.566-46_566-45insAACCACCCATACCC	NP_001157751.1:n.566-46_566-45insAACCACCCATACCC
NM_001164280.1:c.785-46_785-45insAACCACCCATACCC	NP_001157752.1:n.785-46_785-45insAACCACCCATACCC
NM_001467.5:c.785-46_785-45insAACCACCCATACCC	NP_001458.1:n.785-46_785-45insAACCACCCATACCC
NM_001164278.2:c.785-46_785-45insAACCACCCATACCC	NP_001157750.1:n.785-46_785-45insAACCACCCATACCC
NM_001164279.2:c.566-46_566-45insAACCACCCATACCC	NP_001157751.1:n.566-46_566-45insAACCACCCATACCC
NM_001164280.2:c.785-46_785-45insAACCACCCATACCC	NP_001157752.1:n.785-46_785-45insAACCACCCATACCC
NM_001467.6:c.785-46_785-45insAACCACCCATACCC	NP_001458.1:n.785-46_785-45insAACCACCCATACCC
NM_001164277.2:c.785-46_785-45insAACCACCCATACCC MANE Select	NP_001157749.1:n.785-46_785-45insAACCACCCATACCC