Canonical Allele Identifier: CA2793831488

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026733_119026736dup , CM000673.2:g.119026733_119026736dup	GRCh38
NC_000011.9:g.118897443_118897446dup , CM000673.1:g.118897443_118897446dup	GRCh37
NC_000011.8:g.118402653_118402656dup	NCBI36
NG_013331.1:g.9173_9176dup , LRG_187:g.9173_9176dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1014+204_1014+207dup
ENST00000697845.1:n.1142_1145dup
ENST00000697846.1:n.1014+204_1014+207dup
ENST00000697847.1:n.1015-45_1015-42dup
ENST00000697848.1:n.1015-45_1015-42dup
ENST00000697849.1:n.2257_2260dup
ENST00000697850.1:n.1015-45_1015-42dup
ENST00000697851.1:n.2578_2581dup
ENST00000638186.1:n.1089-45_1089-42dup
ENST00000638360.1:n.921-45_921-42dup
ENST00000638925.1:n.1022-45_1022-42dup
ENST00000650539.1:n.1191-45_1191-42dup
ENST00000330775.9:c.785-45_785-42dup	ENSP00000476242.2:n.785-45_785-42dup
ENST00000357590.9:c.785-45_785-42dup	ENSP00000476176.2:n.785-45_785-42dup
ENST00000524428.5:n.1106+204_1106+207dup
ENST00000525039.5:n.1209-45_1209-42dup
ENST00000525102.5:n.1543-45_1543-42dup
ENST00000525372.5:n.786-45_786-42dup
ENST00000526275.5:n.1567-45_1567-42dup
ENST00000527992.5:n.1013-45_1013-42dup
ENST00000529510.5:n.558+204_558+207dup
ENST00000530407.5:n.935-45_935-42dup
ENST00000532085.1:n.3599_3602dup
ENST00000532888.6:n.1284_1287dup
ENST00000538950.5:c.566-45_566-42dup	ENSP00000475991.2:n.566-45_566-42dup
ENST00000545985.5:c.785-45_785-42dup	ENSP00000475241.2:n.785-45_785-42dup
NM_001164277.1:c.785-45_785-42dup , LRG_187t1:c.785-45_785-42dup	NP_001157749.1:n.785-45_785-42dup
NM_001164278.1:c.785-45_785-42dup	NP_001157750.1:n.785-45_785-42dup
NM_001164279.1:c.566-45_566-42dup	NP_001157751.1:n.566-45_566-42dup
NM_001164280.1:c.785-45_785-42dup	NP_001157752.1:n.785-45_785-42dup
NM_001467.5:c.785-45_785-42dup	NP_001458.1:n.785-45_785-42dup
NM_001164278.2:c.785-45_785-42dup	NP_001157750.1:n.785-45_785-42dup
NM_001164279.2:c.566-45_566-42dup	NP_001157751.1:n.566-45_566-42dup
NM_001164280.2:c.785-45_785-42dup	NP_001157752.1:n.785-45_785-42dup
NM_001467.6:c.785-45_785-42dup	NP_001458.1:n.785-45_785-42dup
NM_001164277.2:c.785-45_785-42dup MANE Select	NP_001157749.1:n.785-45_785-42dup