Canonical Allele Identifier: CA477125876

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118897744G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027034G>C , CM000673.2:g.119027034G>C	GRCh38
NC_000011.9:g.118897744G>C , CM000673.1:g.118897744G>C	GRCh37
NC_000011.8:g.118402954G>C	NCBI36
NG_013331.1:g.8872C>G , LRG_187:g.8872C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.917C>G
ENST00000697845.1:n.841C>G
ENST00000697846.1:n.917C>G
ENST00000697847.1:n.917C>G
ENST00000697848.1:n.917C>G
ENST00000697849.1:n.1956C>G
ENST00000697850.1:n.917C>G
ENST00000697851.1:n.2277C>G
ENST00000638186.1:n.991C>G
ENST00000638360.1:n.823C>G
ENST00000638925.1:n.924C>G
ENST00000650539.1:n.1093C>G
ENST00000330775.9:c.687C>G	ENSP00000476242.2:p.Leu229=
ENST00000357590.9:c.687C>G	ENSP00000476176.2:p.Leu229=
ENST00000524428.5:n.1009C>G
ENST00000525039.5:n.1111C>G
ENST00000525102.5:n.1445C>G
ENST00000525372.5:n.688C>G
ENST00000526275.5:n.1469C>G
ENST00000526626.6:n.650C>G
ENST00000527992.5:n.915C>G
ENST00000529510.5:n.461C>G
ENST00000530407.5:n.837C>G
ENST00000532085.1:n.3298C>G
ENST00000532888.6:n.983C>G
ENST00000538950.5:c.468C>G	ENSP00000475991.2:p.Leu156=
ENST00000545985.5:c.687C>G	ENSP00000475241.2:p.Leu229=
NM_001164277.1:c.687C>G , LRG_187t1:c.687C>G	NP_001157749.1:p.Leu229=
NM_001164278.1:c.687C>G	NP_001157750.1:p.Leu229=
NM_001164279.1:c.468C>G	NP_001157751.1:p.Leu156=
NM_001164280.1:c.687C>G	NP_001157752.1:p.Leu229=
NM_001467.5:c.687C>G	NP_001458.1:p.Leu229=
NM_001164278.2:c.687C>G	NP_001157750.1:p.Leu229=
NM_001164279.2:c.468C>G	NP_001157751.1:p.Leu156=
NM_001164280.2:c.687C>G	NP_001157752.1:p.Leu229=
NM_001467.6:c.687C>G	NP_001458.1:p.Leu229=
NM_001164277.2:c.687C>G MANE Select	NP_001157749.1:p.Leu229=