Canonical Allele Identifier: CA477125366

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118897379G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026669G>T , CM000673.2:g.119026669G>T	GRCh38
NC_000011.9:g.118897379G>T , CM000673.1:g.118897379G>T	GRCh37
NC_000011.8:g.118402589G>T	NCBI36
NG_013331.1:g.9237C>A , LRG_187:g.9237C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1014+268C>A
ENST00000697845.1:n.1206C>A
ENST00000697846.1:n.1014+268C>A
ENST00000697847.1:n.1034C>A
ENST00000697848.1:n.1034C>A
ENST00000697849.1:n.2321C>A
ENST00000697850.1:n.1034C>A
ENST00000697851.1:n.2642C>A
ENST00000638186.1:n.1108C>A
ENST00000638360.1:n.940C>A
ENST00000638925.1:n.1041C>A
ENST00000650539.1:n.1210C>A
ENST00000330775.9:c.804C>A	ENSP00000476242.2:p.Ala268=
ENST00000357590.9:c.804C>A	ENSP00000476176.2:p.Ala268=
ENST00000524428.5:n.1106+268C>A
ENST00000525039.5:n.1228C>A
ENST00000525102.5:n.1562C>A
ENST00000525372.5:n.805C>A
ENST00000526275.5:n.1586C>A
ENST00000527992.5:n.1032C>A
ENST00000529510.5:n.558+268C>A
ENST00000530407.5:n.954C>A
ENST00000532085.1:n.3663C>A
ENST00000532888.6:n.1348C>A
ENST00000538950.5:c.585C>A	ENSP00000475991.2:p.Ala195=
ENST00000545985.5:c.804C>A	ENSP00000475241.2:p.Ala268=
NM_001164277.1:c.804C>A , LRG_187t1:c.804C>A	NP_001157749.1:p.Ala268=
NM_001164278.1:c.804C>A	NP_001157750.1:p.Ala268=
NM_001164279.1:c.585C>A	NP_001157751.1:p.Ala195=
NM_001164280.1:c.804C>A	NP_001157752.1:p.Ala268=
NM_001467.5:c.804C>A	NP_001458.1:p.Ala268=
NM_001164278.2:c.804C>A	NP_001157750.1:p.Ala268=
NM_001164279.2:c.585C>A	NP_001157751.1:p.Ala195=
NM_001164280.2:c.804C>A	NP_001157752.1:p.Ala268=
NM_001467.6:c.804C>A	NP_001458.1:p.Ala268=
NM_001164277.2:c.804C>A MANE Select	NP_001157749.1:p.Ala268=