Canonical Allele Identifier: CA6311939

Gene: SLC37A4

Linked Data

• dbSNP Id: rs781958212
• ExAC: 11:118900103 A / C
• MyVariant Identifiers: chr11:g.118900103A>C (hg19) ; chr11:g.119029393A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029393A>C , CM000673.2:g.119029393A>C	GRCh38
NC_000011.9:g.118900103A>C , CM000673.1:g.118900103A>C	GRCh37
NC_000011.8:g.118405313A>C	NCBI36
NG_013331.1:g.6514T>G , LRG_187:g.6514T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.206T>G
ENST00000697846.1:n.206T>G
ENST00000697847.1:n.206T>G
ENST00000697848.1:n.206T>G
ENST00000697849.1:n.450T>G
ENST00000697850.1:n.206T>G
ENST00000697851.1:n.450T>G
ENST00000638186.1:n.280T>G
ENST00000638360.1:n.214T>G
ENST00000638925.1:n.213T>G
ENST00000650539.1:n.382T>G
ENST00000330775.9:c.-24T>G	ENSP00000476242.2:n.-24T>G
ENST00000357590.9:c.-24T>G	ENSP00000476176.2:n.-24T>G
ENST00000525039.5:n.400T>G
ENST00000525102.5:n.734T>G
ENST00000525787.1:n.272T>G
ENST00000526626.6:n.172T>G
ENST00000527992.5:n.204T>G
ENST00000530407.5:n.196T>G
ENST00000532085.1:n.1471T>G
ENST00000532888.6:n.172T>G
ENST00000534384.1:n.197T>G
ENST00000538950.5:c.-173T>G	ENSP00000475991.2:n.-173T>G
ENST00000545985.5:c.-24T>G	ENSP00000475241.2:n.-24T>G
NM_001164277.1:c.-24T>G , LRG_187t1:c.-24T>G	NP_001157749.1:n.-24T>G
NM_001164278.1:c.-24T>G	NP_001157750.1:n.-24T>G
NM_001164279.1:c.-173T>G	NP_001157751.1:n.-173T>G
NM_001164280.1:c.-24T>G	NP_001157752.1:n.-24T>G
NM_001467.5:c.-24T>G	NP_001458.1:n.-24T>G
NM_001164278.2:c.-24T>G	NP_001157750.1:n.-24T>G
NM_001164279.2:c.-173T>G	NP_001157751.1:n.-173T>G
NM_001164280.2:c.-24T>G	NP_001157752.1:n.-24T>G
NM_001467.6:c.-24T>G	NP_001458.1:n.-24T>G
NM_001164277.2:c.-24T>G MANE Select	NP_001157749.1:n.-24T>G