Canonical Allele Identifier: CA10604058

Gene: SLC37A4

Linked Data

• ClinVar Variation Id: 282064
• ClinVar RCV Id: RCV000332634 ; RCV001279136
• dbSNP Id: rs886042302
• gnomAD v2: 11-118896783-A-G
• gnomAD v3: 11-119026073-A-G
• gnomAD v4: 11-119026073-A-G
• MyVariant Identifiers: chr11:g.118896783A>G (hg19) ; chr11:g.119026073A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026073A>G , CM000673.2:g.119026073A>G	GRCh38
NC_000011.9:g.118896783A>G , CM000673.1:g.118896783A>G	GRCh37
NC_000011.8:g.118401993A>G	NCBI36
NG_013331.1:g.9833T>C , LRG_187:g.9833T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1022T>C
ENST00000697845.1:n.1802T>C
ENST00000697846.1:n.1022T>C
ENST00000697847.1:n.1202-316T>C
ENST00000697848.1:n.1108T>C
ENST00000697849.1:n.2917T>C
ENST00000697850.1:n.1108T>C
ENST00000697851.1:n.2716T>C
ENST00000638186.1:n.1182T>C
ENST00000638360.1:n.1014T>C
ENST00000638925.1:n.1147T>C
ENST00000650539.1:n.1284T>C
ENST00000330775.9:c.878T>C	ENSP00000476242.2:p.Leu293Pro
ENST00000357590.9:c.878T>C	ENSP00000476176.2:p.Leu293Pro
ENST00000524428.5:n.1114T>C
ENST00000525039.5:n.1302T>C
ENST00000525102.5:n.1636T>C
ENST00000525372.5:n.976T>C
ENST00000526275.5:n.1660T>C
ENST00000527992.5:n.1106T>C
ENST00000529510.5:n.566T>C
ENST00000530407.5:n.1028T>C
ENST00000532085.1:n.4259T>C
ENST00000538950.5:c.659T>C	ENSP00000475991.2:p.Leu220Pro
ENST00000545985.5:c.878T>C	ENSP00000475241.2:p.Leu293Pro
NM_001164277.1:c.878T>C , LRG_187t1:c.878T>C	NP_001157749.1:p.Leu293Pro
NM_001164278.1:c.878T>C	NP_001157750.1:p.Leu293Pro
NM_001164279.1:c.659T>C	NP_001157751.1:p.Leu220Pro
NM_001164280.1:c.878T>C	NP_001157752.1:p.Leu293Pro
NM_001467.5:c.878T>C	NP_001458.1:p.Leu293Pro
NM_001164278.2:c.878T>C	NP_001157750.1:p.Leu293Pro
NM_001164279.2:c.659T>C	NP_001157751.1:p.Leu220Pro
NM_001164280.2:c.878T>C	NP_001157752.1:p.Leu293Pro
NM_001467.6:c.878T>C	NP_001458.1:p.Leu293Pro
NM_001164277.2:c.878T>C MANE Select	NP_001157749.1:p.Leu293Pro