Canonical Allele Identifier: CA2003776465

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119030370T= , CM000673.2:g.119030370T=	GRCh38
NC_000011.9:g.118901080T= , CM000673.1:g.118901080T=	GRCh37
NC_000011.8:g.118406290T=	NCBI36
NG_013331.1:g.5537A= , LRG_187:g.5537A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.34+479A=
ENST00000697846.1:n.34+479A=
ENST00000697847.1:n.34+479A=
ENST00000697848.1:n.34+479A=
ENST00000697850.1:n.34+479A=
ENST00000638360.1:n.42+479A=
ENST00000638925.1:n.41+479A=
ENST00000650539.1:n.10A=
ENST00000330775.9:c.-196+479A=	ENSP00000476242.2:n.-196+479A=
ENST00000357590.9:c.-196+178A=	ENSP00000476176.2:n.-196+178A=
ENST00000525039.5:n.228+178A=
ENST00000525102.5:n.424A=
ENST00000527992.5:n.32+479A=
ENST00000530407.5:n.24+479A=
ENST00000532085.1:n.494A=
ENST00000538950.5:c.-345+479A=	ENSP00000475991.2:n.-345+479A=
ENST00000545985.5:c.-334A=	ENSP00000475241.2:n.-334A=
NM_001164277.1:c.-334A= , LRG_187t1:c.-334A=	NP_001157749.1:n.-334A=
NM_001164278.1:c.-196+178A=	NP_001157750.1:n.-196+178A=
NM_001164279.1:c.-345+479A=	NP_001157751.1:n.-345+479A=
NM_001467.5:c.-196+479A=	NP_001458.1:n.-196+479A=
NM_001164278.2:c.-196+178A=	NP_001157750.1:n.-196+178A=
NM_001164279.2:c.-345+479A=	NP_001157751.1:n.-345+479A=
NM_001467.6:c.-196+479A=	NP_001458.1:n.-196+479A=
NM_001164277.2:c.-334A= MANE Select	NP_001157749.1:n.-334A=