Canonical Allele Identifier: CA382901581

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118897781A>G (hg19) ; chr11:g.119027071A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027071A>G , CM000673.2:g.119027071A>G	GRCh38
NC_000011.9:g.118897781A>G , CM000673.1:g.118897781A>G	GRCh37
NC_000011.8:g.118402991A>G	NCBI36
NG_013331.1:g.8835T>C , LRG_187:g.8835T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.880T>C
ENST00000697845.1:n.804T>C
ENST00000697846.1:n.880T>C
ENST00000697847.1:n.880T>C
ENST00000697848.1:n.880T>C
ENST00000697849.1:n.1919T>C
ENST00000697850.1:n.880T>C
ENST00000697851.1:n.2240T>C
ENST00000638186.1:n.954T>C
ENST00000638360.1:n.786T>C
ENST00000638925.1:n.887T>C
ENST00000650539.1:n.1056T>C
ENST00000330775.9:c.650T>C	ENSP00000476242.2:p.Leu217Pro
ENST00000357590.9:c.650T>C	ENSP00000476176.2:p.Leu217Pro
ENST00000524428.5:n.972T>C
ENST00000525039.5:n.1074T>C
ENST00000525102.5:n.1408T>C
ENST00000525372.5:n.651T>C
ENST00000526275.5:n.1432T>C
ENST00000526626.6:n.613T>C
ENST00000527992.5:n.878T>C
ENST00000529510.5:n.424T>C
ENST00000530407.5:n.800T>C
ENST00000532085.1:n.3261T>C
ENST00000532888.6:n.946T>C
ENST00000538950.5:c.431T>C	ENSP00000475991.2:p.Leu144Pro
ENST00000545985.5:c.650T>C	ENSP00000475241.2:p.Leu217Pro
NM_001164277.1:c.650T>C , LRG_187t1:c.650T>C	NP_001157749.1:p.Leu217Pro
NM_001164278.1:c.650T>C	NP_001157750.1:p.Leu217Pro
NM_001164279.1:c.431T>C	NP_001157751.1:p.Leu144Pro
NM_001164280.1:c.650T>C	NP_001157752.1:p.Leu217Pro
NM_001467.5:c.650T>C	NP_001458.1:p.Leu217Pro
NM_001164278.2:c.650T>C	NP_001157750.1:p.Leu217Pro
NM_001164279.2:c.431T>C	NP_001157751.1:p.Leu144Pro
NM_001164280.2:c.650T>C	NP_001157752.1:p.Leu217Pro
NM_001467.6:c.650T>C	NP_001458.1:p.Leu217Pro
NM_001164277.2:c.650T>C MANE Select	NP_001157749.1:p.Leu217Pro