Canonical Allele Identifier: CA382905352

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118899009T>C (hg19) ; chr11:g.119028299T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119028299T>C , CM000673.2:g.119028299T>C	GRCh38
NC_000011.9:g.118899009T>C , CM000673.1:g.118899009T>C	GRCh37
NC_000011.8:g.118404219T>C	NCBI36
NG_013331.1:g.7608A>G , LRG_187:g.7608A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.505A>G
ENST00000697845.1:n.429A>G
ENST00000697846.1:n.505A>G
ENST00000697847.1:n.505A>G
ENST00000697848.1:n.505A>G
ENST00000697849.1:n.1544A>G
ENST00000697850.1:n.505A>G
ENST00000697851.1:n.1544A>G
ENST00000638186.1:n.579A>G
ENST00000638360.1:n.513A>G
ENST00000638925.1:n.512A>G
ENST00000650539.1:n.681A>G
ENST00000330775.9:c.276A>G	ENSP00000476242.2:p.Ile92Met
ENST00000357590.9:c.276A>G	ENSP00000476176.2:p.Ile92Met
ENST00000524428.5:n.276A>G
ENST00000525039.5:n.699A>G
ENST00000525102.5:n.1033A>G
ENST00000525372.5:n.276A>G
ENST00000525787.1:n.571A>G
ENST00000526275.5:n.736A>G
ENST00000526626.6:n.344-427A>G
ENST00000527992.5:n.503A>G
ENST00000529510.5:n.294A>G
ENST00000530407.5:n.425A>G
ENST00000532085.1:n.2565A>G
ENST00000532888.6:n.571A>G
ENST00000534384.1:n.496A>G
ENST00000538950.5:c.57A>G	ENSP00000475991.2:p.Ile19Met
ENST00000545985.5:c.276A>G	ENSP00000475241.2:p.Ile92Met
NM_001164277.1:c.276A>G , LRG_187t1:c.276A>G	NP_001157749.1:p.Ile92Met
NM_001164278.1:c.276A>G	NP_001157750.1:p.Ile92Met
NM_001164279.1:c.57A>G	NP_001157751.1:p.Ile19Met
NM_001164280.1:c.276A>G	NP_001157752.1:p.Ile92Met
NM_001467.5:c.276A>G	NP_001458.1:p.Ile92Met
NM_001164278.2:c.276A>G	NP_001157750.1:p.Ile92Met
NM_001164279.2:c.57A>G	NP_001157751.1:p.Ile19Met
NM_001164280.2:c.276A>G	NP_001157752.1:p.Ile92Met
NM_001467.6:c.276A>G	NP_001458.1:p.Ile92Met
NM_001164277.2:c.276A>G MANE Select	NP_001157749.1:p.Ile92Met