Canonical Allele Identifier: CA382904755

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119028243C>T , CM000673.2:g.119028243C>T	GRCh38
NC_000011.9:g.118898953C>T , CM000673.1:g.118898953C>T	GRCh37
NC_000011.8:g.118404163C>T	NCBI36
NG_013331.1:g.7664G>A , LRG_187:g.7664G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001164277.2:c.332G>A MANE Select	NP_001157749.1:p.Gly111Asp
NM_001164277.1:c.332G>A , LRG_187t1:c.332G>A	NP_001157749.1:p.Gly111Asp
NM_001164278.1:c.332G>A	NP_001157750.1:p.Gly111Asp
NM_001164278.2:c.332G>A	NP_001157750.1:p.Gly111Asp
NM_001164279.1:c.113G>A	NP_001157751.1:p.Gly38Asp
NM_001164279.2:c.113G>A	NP_001157751.1:p.Gly38Asp
NM_001164280.1:c.332G>A	NP_001157752.1:p.Gly111Asp
NM_001164280.2:c.332G>A	NP_001157752.1:p.Gly111Asp
NM_001467.5:c.332G>A	NP_001458.1:p.Gly111Asp
NM_001467.6:c.332G>A	NP_001458.1:p.Gly111Asp
ENST00000330775.9:c.332G>A	ENSP00000476242.2:p.Gly111Asp
ENST00000357590.9:c.332G>A	ENSP00000476176.2:p.Gly111Asp
ENST00000524428.5:n.332G>A
ENST00000525039.5:n.755G>A
ENST00000525102.5:n.1089G>A
ENST00000525372.5:n.332G>A
ENST00000525787.1:n.627G>A
ENST00000526275.5:n.792G>A
ENST00000526626.6:n.344-371G>A
ENST00000527992.5:n.559G>A
ENST00000529510.5:n.350G>A
ENST00000529510.6:n.561G>A
ENST00000530407.5:n.481G>A
ENST00000532085.1:n.2621G>A
ENST00000532888.6:n.627G>A
ENST00000534384.1:n.552G>A
ENST00000538950.5:c.113G>A	ENSP00000475991.2:p.Gly38Asp
ENST00000545985.5:c.332G>A	ENSP00000475241.2:p.Gly111Asp
ENST00000638186.1:n.635G>A
ENST00000638360.1:n.569G>A
ENST00000638925.1:n.568G>A
ENST00000650539.1:n.737G>A
ENST00000697845.1:n.485G>A
ENST00000697846.1:n.561G>A
ENST00000697847.1:n.561G>A
ENST00000697848.1:n.561G>A
ENST00000697849.1:n.1600G>A
ENST00000697850.1:n.561G>A
ENST00000697851.1:n.1600G>A