Canonical Allele Identifier: CA2575003440

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029403C>T , CM000673.2:g.119029403C>T	GRCh38
NC_000011.9:g.118900113C>T , CM000673.1:g.118900113C>T	GRCh37
NC_000011.8:g.118405323C>T	NCBI36
NG_013331.1:g.6504G>A , LRG_187:g.6504G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.196G>A
ENST00000697846.1:n.196G>A
ENST00000697847.1:n.196G>A
ENST00000697848.1:n.196G>A
ENST00000697849.1:n.440G>A
ENST00000697850.1:n.196G>A
ENST00000697851.1:n.440G>A
ENST00000638186.1:n.270G>A
ENST00000638360.1:n.204G>A
ENST00000638925.1:n.203G>A
ENST00000650539.1:n.372G>A
ENST00000330775.9:c.-34G>A	ENSP00000476242.2:n.-34G>A
ENST00000357590.9:c.-34G>A	ENSP00000476176.2:n.-34G>A
ENST00000525039.5:n.390G>A
ENST00000525102.5:n.724G>A
ENST00000525787.1:n.262G>A
ENST00000526626.6:n.162G>A
ENST00000527992.5:n.194G>A
ENST00000530407.5:n.186G>A
ENST00000532085.1:n.1461G>A
ENST00000532888.6:n.162G>A
ENST00000534384.1:n.187G>A
ENST00000538950.5:c.-183G>A	ENSP00000475991.2:n.-183G>A
ENST00000545985.5:c.-34G>A	ENSP00000475241.2:n.-34G>A
NM_001164277.1:c.-34G>A , LRG_187t1:c.-34G>A	NP_001157749.1:n.-34G>A
NM_001164278.1:c.-34G>A	NP_001157750.1:n.-34G>A
NM_001164279.1:c.-183G>A	NP_001157751.1:n.-183G>A
NM_001164280.1:c.-34G>A	NP_001157752.1:n.-34G>A
NM_001467.5:c.-34G>A	NP_001458.1:n.-34G>A
NM_001164278.2:c.-34G>A	NP_001157750.1:n.-34G>A
NM_001164279.2:c.-183G>A	NP_001157751.1:n.-183G>A
NM_001164280.2:c.-34G>A	NP_001157752.1:n.-34G>A
NM_001467.6:c.-34G>A	NP_001458.1:n.-34G>A
NM_001164277.2:c.-34G>A MANE Select	NP_001157749.1:n.-34G>A