Canonical Allele Identifier: CA477126636

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119028236G>A , CM000673.2:g.119028236G>A	GRCh38
NC_000011.9:g.118898946G>A , CM000673.1:g.118898946G>A	GRCh37
NC_000011.8:g.118404156G>A	NCBI36
NG_013331.1:g.7671C>T , LRG_187:g.7671C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001164277.2:c.339C>T MANE Select	NP_001157749.1:p.Ala113=
NM_001164277.1:c.339C>T , LRG_187t1:c.339C>T	NP_001157749.1:p.Ala113=
NM_001164278.1:c.339C>T	NP_001157750.1:p.Ala113=
NM_001164278.2:c.339C>T	NP_001157750.1:p.Ala113=
NM_001164279.1:c.120C>T	NP_001157751.1:p.Ala40=
NM_001164279.2:c.120C>T	NP_001157751.1:p.Ala40=
NM_001164280.1:c.339C>T	NP_001157752.1:p.Ala113=
NM_001164280.2:c.339C>T	NP_001157752.1:p.Ala113=
NM_001467.5:c.339C>T	NP_001458.1:p.Ala113=
NM_001467.6:c.339C>T	NP_001458.1:p.Ala113=
ENST00000330775.9:c.339C>T	ENSP00000476242.2:p.Ala113=
ENST00000357590.9:c.339C>T	ENSP00000476176.2:p.Ala113=
ENST00000524428.5:n.339C>T
ENST00000525039.5:n.762C>T
ENST00000525102.5:n.1096C>T
ENST00000525372.5:n.339C>T
ENST00000525787.1:n.634C>T
ENST00000526275.5:n.799C>T
ENST00000526626.6:n.344-364C>T
ENST00000527992.5:n.566C>T
ENST00000529510.5:n.357C>T
ENST00000529510.6:n.568C>T
ENST00000530407.5:n.488C>T
ENST00000532085.1:n.2628C>T
ENST00000532888.6:n.634C>T
ENST00000538950.5:c.120C>T	ENSP00000475991.2:p.Ala40=
ENST00000545985.5:c.339C>T	ENSP00000475241.2:p.Ala113=
ENST00000638186.1:n.642C>T
ENST00000638360.1:n.576C>T
ENST00000638925.1:n.575C>T
ENST00000650539.1:n.744C>T
ENST00000697845.1:n.492C>T
ENST00000697846.1:n.568C>T
ENST00000697847.1:n.568C>T
ENST00000697848.1:n.568C>T
ENST00000697849.1:n.1607C>T
ENST00000697850.1:n.568C>T
ENST00000697851.1:n.1607C>T