Canonical Allele Identifier: CA2003775522

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029488C= , CM000673.2:g.119029488C=	GRCh38
NC_000011.9:g.118900198C= , CM000673.1:g.118900198C=	GRCh37
NC_000011.8:g.118405408C=	NCBI36
NG_013331.1:g.6419G= , LRG_187:g.6419G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.111G=
ENST00000697846.1:n.111G=
ENST00000697847.1:n.111G=
ENST00000697848.1:n.111G=
ENST00000697849.1:n.355G=
ENST00000697850.1:n.111G=
ENST00000697851.1:n.355G=
ENST00000638186.1:n.185G=
ENST00000638360.1:n.119G=
ENST00000638925.1:n.118G=
ENST00000650539.1:n.287G=
ENST00000330775.9:c.-119G=	ENSP00000476242.2:n.-119G=
ENST00000357590.9:c.-119G=	ENSP00000476176.2:n.-119G=
ENST00000525039.5:n.305G=
ENST00000525102.5:n.639G=
ENST00000525787.1:n.177G=
ENST00000526626.6:n.77G=
ENST00000527992.5:n.109G=
ENST00000530407.5:n.101G=
ENST00000532085.1:n.1376G=
ENST00000532888.6:n.77G=
ENST00000534384.1:n.102G=
ENST00000538950.5:c.-268G=	ENSP00000475991.2:n.-268G=
ENST00000545985.5:c.-119G=	ENSP00000475241.2:n.-119G=
NM_001164277.1:c.-119G= , LRG_187t1:c.-119G=	NP_001157749.1:n.-119G=
NM_001164278.1:c.-119G=	NP_001157750.1:n.-119G=
NM_001164279.1:c.-268G=	NP_001157751.1:n.-268G=
NM_001164280.1:c.-119G=	NP_001157752.1:n.-119G=
NM_001467.5:c.-119G=	NP_001458.1:n.-119G=
NM_001164278.2:c.-119G=	NP_001157750.1:n.-119G=
NM_001164279.2:c.-268G=	NP_001157751.1:n.-268G=
NM_001467.6:c.-119G=	NP_001458.1:n.-119G=
NM_001164277.2:c.-119G= MANE Select	NP_001157749.1:n.-119G=