Canonical Allele Identifier: CA2574999788

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119028166T>G , CM000673.2:g.119028166T>G	GRCh38
NC_000011.9:g.118898876T>G , CM000673.1:g.118898876T>G	GRCh37
NC_000011.8:g.118404086T>G	NCBI36
NG_013331.1:g.7741A>C , LRG_187:g.7741A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.610+28A>C
ENST00000697845.1:n.534+28A>C
ENST00000697846.1:n.610+28A>C
ENST00000697847.1:n.610+28A>C
ENST00000697848.1:n.610+28A>C
ENST00000697849.1:n.1649+28A>C
ENST00000697850.1:n.610+28A>C
ENST00000697851.1:n.1677A>C
ENST00000638186.1:n.684+28A>C
ENST00000638360.1:n.618+28A>C
ENST00000638925.1:n.617+28A>C
ENST00000650539.1:n.786+28A>C
ENST00000330775.9:c.381+28A>C	ENSP00000476242.2:n.381+28A>C
ENST00000357590.9:c.381+28A>C	ENSP00000476176.2:n.381+28A>C
ENST00000524428.5:n.409A>C
ENST00000525039.5:n.804+28A>C
ENST00000525102.5:n.1138+28A>C
ENST00000525372.5:n.381+28A>C
ENST00000525787.1:n.704A>C
ENST00000526275.5:n.869A>C
ENST00000526626.6:n.344-294A>C
ENST00000527992.5:n.608+28A>C
ENST00000529510.5:n.399+28A>C
ENST00000530407.5:n.530+28A>C
ENST00000532085.1:n.2698A>C
ENST00000532888.6:n.676+28A>C
ENST00000538950.5:c.162+28A>C	ENSP00000475991.2:n.162+28A>C
ENST00000545985.5:c.381+28A>C	ENSP00000475241.2:n.381+28A>C
NM_001164277.1:c.381+28A>C , LRG_187t1:c.381+28A>C	NP_001157749.1:n.381+28A>C
NM_001164278.1:c.381+28A>C	NP_001157750.1:n.381+28A>C
NM_001164279.1:c.162+28A>C	NP_001157751.1:n.162+28A>C
NM_001164280.1:c.381+28A>C	NP_001157752.1:n.381+28A>C
NM_001467.5:c.381+28A>C	NP_001458.1:n.381+28A>C
NM_001164278.2:c.381+28A>C	NP_001157750.1:n.381+28A>C
NM_001164279.2:c.162+28A>C	NP_001157751.1:n.162+28A>C
NM_001164280.2:c.381+28A>C	NP_001157752.1:n.381+28A>C
NM_001467.6:c.381+28A>C	NP_001458.1:n.381+28A>C
NM_001164277.2:c.381+28A>C MANE Select	NP_001157749.1:n.381+28A>C