Canonical Allele Identifier: CA2003775535

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029509T= , CM000673.2:g.119029509T=	GRCh38
NC_000011.9:g.118900219T= , CM000673.1:g.118900219T=	GRCh37
NC_000011.8:g.118405429T=	NCBI36
NG_013331.1:g.6398A= , LRG_187:g.6398A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.90A=
ENST00000697846.1:n.90A=
ENST00000697847.1:n.90A=
ENST00000697848.1:n.90A=
ENST00000697849.1:n.334A=
ENST00000697850.1:n.90A=
ENST00000697851.1:n.334A=
ENST00000638186.1:n.164A=
ENST00000638360.1:n.98A=
ENST00000638925.1:n.97A=
ENST00000650539.1:n.266A=
ENST00000330775.9:c.-140A=	ENSP00000476242.2:n.-140A=
ENST00000357590.9:c.-140A=	ENSP00000476176.2:n.-140A=
ENST00000525039.5:n.284A=
ENST00000525102.5:n.618A=
ENST00000525787.1:n.156A=
ENST00000526626.6:n.56A=
ENST00000527992.5:n.88A=
ENST00000530407.5:n.80A=
ENST00000532085.1:n.1355A=
ENST00000532888.6:n.56A=
ENST00000534384.1:n.81A=
ENST00000538950.5:c.-289A=	ENSP00000475991.2:n.-289A=
ENST00000545985.5:c.-140A=	ENSP00000475241.2:n.-140A=
NM_001164277.1:c.-140A= , LRG_187t1:c.-140A=	NP_001157749.1:n.-140A=
NM_001164278.1:c.-140A=	NP_001157750.1:n.-140A=
NM_001164279.1:c.-289A=	NP_001157751.1:n.-289A=
NM_001164280.1:c.-140A=	NP_001157752.1:n.-140A=
NM_001467.5:c.-140A=	NP_001458.1:n.-140A=
NM_001164278.2:c.-140A=	NP_001157750.1:n.-140A=
NM_001164279.2:c.-289A=	NP_001157751.1:n.-289A=
NM_001467.6:c.-140A=	NP_001458.1:n.-140A=
NM_001164277.2:c.-140A= MANE Select	NP_001157749.1:n.-140A=