Canonical Allele Identifier: CA382899898

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119026607-G-T
• MyVariant Identifiers: chr11:g.118897317G>T (hg19) ; chr11:g.119026607G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026607G>T , CM000673.2:g.119026607G>T	GRCh38
NC_000011.9:g.118897317G>T , CM000673.1:g.118897317G>T	GRCh37
NC_000011.8:g.118402527G>T	NCBI36
NG_013331.1:g.9299C>A , LRG_187:g.9299C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1014+330C>A
ENST00000697845.1:n.1268C>A
ENST00000697846.1:n.1014+330C>A
ENST00000697847.1:n.1096C>A
ENST00000697848.1:n.1096C>A
ENST00000697849.1:n.2383C>A
ENST00000697850.1:n.1096C>A
ENST00000697851.1:n.2704C>A
ENST00000638186.1:n.1170C>A
ENST00000638360.1:n.1002C>A
ENST00000638925.1:n.1103C>A
ENST00000650539.1:n.1272C>A
ENST00000330775.9:c.866C>A	ENSP00000476242.2:p.Ala289Glu
ENST00000357590.9:c.866C>A	ENSP00000476176.2:p.Ala289Glu
ENST00000524428.5:n.1106+330C>A
ENST00000525039.5:n.1290C>A
ENST00000525102.5:n.1624C>A
ENST00000525372.5:n.867C>A
ENST00000526275.5:n.1648C>A
ENST00000527992.5:n.1094C>A
ENST00000529510.5:n.558+330C>A
ENST00000530407.5:n.1016C>A
ENST00000532085.1:n.3725C>A
ENST00000538950.5:c.647C>A	ENSP00000475991.2:p.Ala216Glu
ENST00000545985.5:c.866C>A	ENSP00000475241.2:p.Ala289Glu
NM_001164277.1:c.866C>A , LRG_187t1:c.866C>A	NP_001157749.1:p.Ala289Glu
NM_001164278.1:c.866C>A	NP_001157750.1:p.Ala289Glu
NM_001164279.1:c.647C>A	NP_001157751.1:p.Ala216Glu
NM_001164280.1:c.866C>A	NP_001157752.1:p.Ala289Glu
NM_001467.5:c.866C>A	NP_001458.1:p.Ala289Glu
NM_001164278.2:c.866C>A	NP_001157750.1:p.Ala289Glu
NM_001164279.2:c.647C>A	NP_001157751.1:p.Ala216Glu
NM_001164280.2:c.866C>A	NP_001157752.1:p.Ala289Glu
NM_001467.6:c.866C>A	NP_001458.1:p.Ala289Glu
NM_001164277.2:c.866C>A MANE Select	NP_001157749.1:p.Ala289Glu