Canonical Allele Identifier: CA229599156

Gene: SLC37A4

Linked Data

• dbSNP Id: rs575985730
• gnomAD v3: 11-119027766-T-G
• gnomAD v4: 11-119027766-T-G
• MyVariant Identifiers: chr11:g.118898476T>G (hg19) ; chr11:g.119027766T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027766T>G , CM000673.2:g.119027766T>G	GRCh38
NC_000011.9:g.118898476T>G , CM000673.1:g.118898476T>G	GRCh37
NC_000011.8:g.118403686T>G	NCBI36
NG_013331.1:g.8141A>C , LRG_187:g.8141A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.717A>C
ENST00000697845.1:n.641A>C
ENST00000697846.1:n.717A>C
ENST00000697847.1:n.717A>C
ENST00000697848.1:n.717A>C
ENST00000697849.1:n.1756A>C
ENST00000697850.1:n.717A>C
ENST00000697851.1:n.2077A>C
ENST00000638186.1:n.791A>C
ENST00000638360.1:n.623A>C
ENST00000638925.1:n.724A>C
ENST00000650539.1:n.893A>C
ENST00000330775.9:c.488A>C	ENSP00000476242.2:p.Tyr163Ser
ENST00000357590.9:c.488A>C	ENSP00000476176.2:p.Tyr163Ser
ENST00000524428.5:n.809A>C
ENST00000525039.5:n.911A>C
ENST00000525102.5:n.1245A>C
ENST00000525372.5:n.488A>C
ENST00000526275.5:n.1269A>C
ENST00000526626.6:n.450A>C
ENST00000527992.5:n.715A>C
ENST00000529510.5:n.399+428A>C
ENST00000530407.5:n.637A>C
ENST00000532085.1:n.3098A>C
ENST00000532888.6:n.783A>C
ENST00000538950.5:c.269A>C	ENSP00000475991.2:p.Tyr90Ser
ENST00000545985.5:c.488A>C	ENSP00000475241.2:p.Tyr163Ser
NM_001164277.1:c.488A>C , LRG_187t1:c.488A>C	NP_001157749.1:p.Tyr163Ser
NM_001164278.1:c.488A>C	NP_001157750.1:p.Tyr163Ser
NM_001164279.1:c.269A>C	NP_001157751.1:p.Tyr90Ser
NM_001164280.1:c.488A>C	NP_001157752.1:p.Tyr163Ser
NM_001467.5:c.488A>C	NP_001458.1:p.Tyr163Ser
NM_001164278.2:c.488A>C	NP_001157750.1:p.Tyr163Ser
NM_001164279.2:c.269A>C	NP_001157751.1:p.Tyr90Ser
NM_001164280.2:c.488A>C	NP_001157752.1:p.Tyr163Ser
NM_001467.6:c.488A>C	NP_001458.1:p.Tyr163Ser
NM_001164277.2:c.488A>C MANE Select	NP_001157749.1:p.Tyr163Ser