Canonical Allele Identifier: CA2003776020

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029964C= , CM000673.2:g.119029964C=	GRCh38
NC_000011.9:g.118900674C= , CM000673.1:g.118900674C=	GRCh37
NC_000011.8:g.118405884C=	NCBI36
NG_013331.1:g.5943G= , LRG_187:g.5943G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.35-400G=
ENST00000697846.1:n.35-400G=
ENST00000697847.1:n.35-400G=
ENST00000697848.1:n.35-400G=
ENST00000697850.1:n.35-400G=
ENST00000638186.1:n.11G=
ENST00000638360.1:n.43-400G=
ENST00000638925.1:n.42-400G=
ENST00000650539.1:n.210+206G=
ENST00000330775.9:c.-195-400G=	ENSP00000476242.2:n.-195-400G=
ENST00000357590.9:c.-195-400G=	ENSP00000476176.2:n.-195-400G=
ENST00000525039.5:n.229-400G=
ENST00000525102.5:n.562+268G=
ENST00000527992.5:n.33-400G=
ENST00000530407.5:n.25-400G=
ENST00000532085.1:n.900G=
ENST00000538950.5:c.-344-400G=	ENSP00000475991.2:n.-344-400G=
ENST00000545985.5:c.-196+268G=	ENSP00000475241.2:n.-196+268G=
NM_001164277.1:c.-196+268G= , LRG_187t1:c.-196+268G=	NP_001157749.1:n.-196+268G=
NM_001164278.1:c.-195-400G=	NP_001157750.1:n.-195-400G=
NM_001164279.1:c.-344-400G=	NP_001157751.1:n.-344-400G=
NM_001467.5:c.-195-400G=	NP_001458.1:n.-195-400G=
NM_001164278.2:c.-195-400G=	NP_001157750.1:n.-195-400G=
NM_001164279.2:c.-344-400G=	NP_001157751.1:n.-344-400G=
NM_001467.6:c.-195-400G=	NP_001458.1:n.-195-400G=
NM_001164277.2:c.-196+268G= MANE Select	NP_001157749.1:n.-196+268G=