Canonical Allele Identifier: CA382905262

Gene: SLC37A4

Linked Data

• dbSNP Id: rs1366233244
• MyVariant Identifiers: chr11:g.118899002C>A (hg19) ; chr11:g.119028292C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119028292C>A , CM000673.2:g.119028292C>A	GRCh38
NC_000011.9:g.118899002C>A , CM000673.1:g.118899002C>A	GRCh37
NC_000011.8:g.118404212C>A	NCBI36
NG_013331.1:g.7615G>T , LRG_187:g.7615G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.512G>T
ENST00000697845.1:n.436G>T
ENST00000697846.1:n.512G>T
ENST00000697847.1:n.512G>T
ENST00000697848.1:n.512G>T
ENST00000697849.1:n.1551G>T
ENST00000697850.1:n.512G>T
ENST00000697851.1:n.1551G>T
ENST00000638186.1:n.586G>T
ENST00000638360.1:n.520G>T
ENST00000638925.1:n.519G>T
ENST00000650539.1:n.688G>T
ENST00000330775.9:c.283G>T	ENSP00000476242.2:p.Ala95Ser
ENST00000357590.9:c.283G>T	ENSP00000476176.2:p.Ala95Ser
ENST00000524428.5:n.283G>T
ENST00000525039.5:n.706G>T
ENST00000525102.5:n.1040G>T
ENST00000525372.5:n.283G>T
ENST00000525787.1:n.578G>T
ENST00000526275.5:n.743G>T
ENST00000526626.6:n.344-420G>T
ENST00000527992.5:n.510G>T
ENST00000529510.5:n.301G>T
ENST00000530407.5:n.432G>T
ENST00000532085.1:n.2572G>T
ENST00000532888.6:n.578G>T
ENST00000534384.1:n.503G>T
ENST00000538950.5:c.64G>T	ENSP00000475991.2:p.Ala22Ser
ENST00000545985.5:c.283G>T	ENSP00000475241.2:p.Ala95Ser
NM_001164277.1:c.283G>T , LRG_187t1:c.283G>T	NP_001157749.1:p.Ala95Ser
NM_001164278.1:c.283G>T	NP_001157750.1:p.Ala95Ser
NM_001164279.1:c.64G>T	NP_001157751.1:p.Ala22Ser
NM_001164280.1:c.283G>T	NP_001157752.1:p.Ala95Ser
NM_001467.5:c.283G>T	NP_001458.1:p.Ala95Ser
NM_001164278.2:c.283G>T	NP_001157750.1:p.Ala95Ser
NM_001164279.2:c.64G>T	NP_001157751.1:p.Ala22Ser
NM_001164280.2:c.283G>T	NP_001157752.1:p.Ala95Ser
NM_001467.6:c.283G>T	NP_001458.1:p.Ala95Ser
NM_001164277.2:c.283G>T MANE Select	NP_001157749.1:p.Ala95Ser