Canonical Allele Identifier: CA2003749821

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027968A= , CM000673.2:g.119027968A=	GRCh38
NC_000011.9:g.118898678A= , CM000673.1:g.118898678A=	GRCh37
NC_000011.8:g.118403888A=	NCBI36
NG_013331.1:g.7939T= , LRG_187:g.7939T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.611-96T=
ENST00000697845.1:n.535-96T=
ENST00000697846.1:n.611-96T=
ENST00000697847.1:n.611-96T=
ENST00000697848.1:n.611-96T=
ENST00000697849.1:n.1650-96T=
ENST00000697850.1:n.611-96T=
ENST00000697851.1:n.1875T=
ENST00000638186.1:n.685-96T=
ENST00000638360.1:n.619-198T=
ENST00000638925.1:n.618-96T=
ENST00000650539.1:n.787-96T=
ENST00000330775.9:c.382-96T=	ENSP00000476242.2:n.382-96T=
ENST00000357590.9:c.382-96T=	ENSP00000476176.2:n.382-96T=
ENST00000524428.5:n.607T=
ENST00000525039.5:n.805-96T=
ENST00000525102.5:n.1139-96T=
ENST00000525372.5:n.382-96T=
ENST00000525787.1:n.902T=
ENST00000526275.5:n.1067T=
ENST00000526626.6:n.344-96T=
ENST00000527992.5:n.609-96T=
ENST00000529510.5:n.399+226T=
ENST00000530407.5:n.531-96T=
ENST00000532085.1:n.2896T=
ENST00000532888.6:n.677-96T=
ENST00000538950.5:c.163-96T=	ENSP00000475991.2:n.163-96T=
ENST00000545985.5:c.382-96T=	ENSP00000475241.2:n.382-96T=
NM_001164277.1:c.382-96T= , LRG_187t1:c.382-96T=	NP_001157749.1:n.382-96T=
NM_001164278.1:c.382-96T=	NP_001157750.1:n.382-96T=
NM_001164279.1:c.163-96T=	NP_001157751.1:n.163-96T=
NM_001164280.1:c.382-96T=	NP_001157752.1:n.382-96T=
NM_001467.5:c.382-96T=	NP_001458.1:n.382-96T=
NM_001164278.2:c.382-96T=	NP_001157750.1:n.382-96T=
NM_001164279.2:c.163-96T=	NP_001157751.1:n.163-96T=
NM_001164280.2:c.382-96T=	NP_001157752.1:n.382-96T=
NM_001467.6:c.382-96T=	NP_001458.1:n.382-96T=
NM_001164277.2:c.382-96T= MANE Select	NP_001157749.1:n.382-96T=