Canonical Allele Identifier: CA477125717

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118897651A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026941A>T , CM000673.2:g.119026941A>T	GRCh38
NC_000011.9:g.118897651A>T , CM000673.1:g.118897651A>T	GRCh37
NC_000011.8:g.118402861A>T	NCBI36
NG_013331.1:g.8965T>A , LRG_187:g.8965T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.1010T>A
ENST00000697845.1:n.934T>A
ENST00000697846.1:n.1010T>A
ENST00000697847.1:n.1010T>A
ENST00000697848.1:n.1010T>A
ENST00000697849.1:n.2049T>A
ENST00000697850.1:n.1010T>A
ENST00000697851.1:n.2370T>A
ENST00000638186.1:n.1084T>A
ENST00000638360.1:n.916T>A
ENST00000638925.1:n.1017T>A
ENST00000650539.1:n.1186T>A
ENST00000330775.9:c.780T>A	ENSP00000476242.2:p.Leu260=
ENST00000357590.9:c.780T>A	ENSP00000476176.2:p.Leu260=
ENST00000524428.5:n.1102T>A
ENST00000525039.5:n.1204T>A
ENST00000525102.5:n.1538T>A
ENST00000525372.5:n.781T>A
ENST00000526275.5:n.1562T>A
ENST00000527992.5:n.1008T>A
ENST00000529510.5:n.554T>A
ENST00000530407.5:n.930T>A
ENST00000532085.1:n.3391T>A
ENST00000532888.6:n.1076T>A
ENST00000538950.5:c.561T>A	ENSP00000475991.2:p.Leu187=
ENST00000545985.5:c.780T>A	ENSP00000475241.2:p.Leu260=
NM_001164277.1:c.780T>A , LRG_187t1:c.780T>A	NP_001157749.1:p.Leu260=
NM_001164278.1:c.780T>A	NP_001157750.1:p.Leu260=
NM_001164279.1:c.561T>A	NP_001157751.1:p.Leu187=
NM_001164280.1:c.780T>A	NP_001157752.1:p.Leu260=
NM_001467.5:c.780T>A	NP_001458.1:p.Leu260=
NM_001164278.2:c.780T>A	NP_001157750.1:p.Leu260=
NM_001164279.2:c.561T>A	NP_001157751.1:p.Leu187=
NM_001164280.2:c.780T>A	NP_001157752.1:p.Leu260=
NM_001467.6:c.780T>A	NP_001458.1:p.Leu260=
NM_001164277.2:c.780T>A MANE Select	NP_001157749.1:p.Leu260=