Canonical Allele Identifier: CA382899976

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118897328G>T (hg19) ; chr11:g.119026618G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026618G>T , CM000673.2:g.119026618G>T	GRCh38
NC_000011.9:g.118897328G>T , CM000673.1:g.118897328G>T	GRCh37
NC_000011.8:g.118402538G>T	NCBI36
NG_013331.1:g.9288C>A , LRG_187:g.9288C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1014+319C>A
ENST00000697845.1:n.1257C>A
ENST00000697846.1:n.1014+319C>A
ENST00000697847.1:n.1085C>A
ENST00000697848.1:n.1085C>A
ENST00000697849.1:n.2372C>A
ENST00000697850.1:n.1085C>A
ENST00000697851.1:n.2693C>A
ENST00000638186.1:n.1159C>A
ENST00000638360.1:n.991C>A
ENST00000638925.1:n.1092C>A
ENST00000650539.1:n.1261C>A
ENST00000330775.9:c.855C>A	ENSP00000476242.2:p.Asp285Glu
ENST00000357590.9:c.855C>A	ENSP00000476176.2:p.Asp285Glu
ENST00000524428.5:n.1106+319C>A
ENST00000525039.5:n.1279C>A
ENST00000525102.5:n.1613C>A
ENST00000525372.5:n.856C>A
ENST00000526275.5:n.1637C>A
ENST00000527992.5:n.1083C>A
ENST00000529510.5:n.558+319C>A
ENST00000530407.5:n.1005C>A
ENST00000532085.1:n.3714C>A
ENST00000538950.5:c.636C>A	ENSP00000475991.2:p.Asp212Glu
ENST00000545985.5:c.855C>A	ENSP00000475241.2:p.Asp285Glu
NM_001164277.1:c.855C>A , LRG_187t1:c.855C>A	NP_001157749.1:p.Asp285Glu
NM_001164278.1:c.855C>A	NP_001157750.1:p.Asp285Glu
NM_001164279.1:c.636C>A	NP_001157751.1:p.Asp212Glu
NM_001164280.1:c.855C>A	NP_001157752.1:p.Asp285Glu
NM_001467.5:c.855C>A	NP_001458.1:p.Asp285Glu
NM_001164278.2:c.855C>A	NP_001157750.1:p.Asp285Glu
NM_001164279.2:c.636C>A	NP_001157751.1:p.Asp212Glu
NM_001164280.2:c.855C>A	NP_001157752.1:p.Asp285Glu
NM_001467.6:c.855C>A	NP_001458.1:p.Asp285Glu
NM_001164277.2:c.855C>A MANE Select	NP_001157749.1:p.Asp285Glu