Canonical Allele Identifier: CA2003748839

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026022_119026024delinsCCA , CM000673.2:g.119026022_119026024delinsCCA	GRCh38
NC_000011.9:g.118896732_118896734delinsCCA , CM000673.1:g.118896732_118896734delinsCCA	GRCh37
NC_000011.8:g.118401942_118401944delinsCCA	NCBI36
NG_013331.1:g.9882_9884delinsTGG , LRG_187:g.9882_9884delinsTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1071_1073delinsTGG
ENST00000697845.1:n.1851_1853delinsTGG
ENST00000697846.1:n.1071_1073delinsTGG
ENST00000697847.1:n.1202-267_1202-265delinsTGG
ENST00000697848.1:n.1157_1159delinsTGG
ENST00000697849.1:n.2966_2968delinsTGG
ENST00000697850.1:n.1157_1159delinsTGG
ENST00000697851.1:n.2765_2767delinsTGG
ENST00000638186.1:n.1231_1233delinsTGG
ENST00000638360.1:n.1063_1065delinsTGG
ENST00000638925.1:n.1196_1198delinsTGG
ENST00000650539.1:n.1333_1335delinsTGG
ENST00000330775.9:c.927_929delinsTGG	ENSP00000476242.2:p.Ala309=
ENST00000357590.9:c.927_929delinsTGG	ENSP00000476176.2:p.Ala309=
ENST00000524428.5:n.1163_1165delinsTGG
ENST00000525039.5:n.1351_1353delinsTGG
ENST00000525102.5:n.1685_1687delinsTGG
ENST00000525372.5:n.1025_1027delinsTGG
ENST00000526275.5:n.1709_1711delinsTGG
ENST00000527992.5:n.1155_1157delinsTGG
ENST00000529510.5:n.615_617delinsTGG
ENST00000530407.5:n.1077_1079delinsTGG
ENST00000532085.1:n.4308_4310delinsTGG
ENST00000538950.5:c.708_710delinsTGG	ENSP00000475991.2:p.Ala236=
ENST00000545985.5:c.927_929delinsTGG	ENSP00000475241.2:p.Ala309=
NM_001164277.1:c.927_929delinsTGG , LRG_187t1:c.927_929delinsTGG	NP_001157749.1:p.Ala309=
NM_001164278.1:c.927_929delinsTGG	NP_001157750.1:p.Ala309=
NM_001164279.1:c.708_710delinsTGG	NP_001157751.1:p.Ala236=
NM_001164280.1:c.927_929delinsTGG	NP_001157752.1:p.Ala309=
NM_001467.5:c.927_929delinsTGG	NP_001458.1:p.Ala309=
NM_001164278.2:c.927_929delinsTGG	NP_001157750.1:p.Ala309=
NM_001164279.2:c.708_710delinsTGG	NP_001157751.1:p.Ala236=
NM_001164280.2:c.927_929delinsTGG	NP_001157752.1:p.Ala309=
NM_001467.6:c.927_929delinsTGG	NP_001458.1:p.Ala309=
NM_001164277.2:c.927_929delinsTGG MANE Select	NP_001157749.1:p.Ala309=