Canonical Allele Identifier: CA2003749994

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119028288C= , CM000673.2:g.119028288C=	GRCh38
NC_000011.9:g.118898998C= , CM000673.1:g.118898998C=	GRCh37
NC_000011.8:g.118404208C=	NCBI36
NG_013331.1:g.7619G= , LRG_187:g.7619G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.516G=
ENST00000697845.1:n.440G=
ENST00000697846.1:n.516G=
ENST00000697847.1:n.516G=
ENST00000697848.1:n.516G=
ENST00000697849.1:n.1555G=
ENST00000697850.1:n.516G=
ENST00000697851.1:n.1555G=
ENST00000638186.1:n.590G=
ENST00000638360.1:n.524G=
ENST00000638925.1:n.523G=
ENST00000650539.1:n.692G=
ENST00000330775.9:c.287G=	ENSP00000476242.2:p.Trp96=
ENST00000357590.9:c.287G=	ENSP00000476176.2:p.Trp96=
ENST00000524428.5:n.287G=
ENST00000525039.5:n.710G=
ENST00000525102.5:n.1044G=
ENST00000525372.5:n.287G=
ENST00000525787.1:n.582G=
ENST00000526275.5:n.747G=
ENST00000526626.6:n.344-416G=
ENST00000527992.5:n.514G=
ENST00000529510.5:n.305G=
ENST00000530407.5:n.436G=
ENST00000532085.1:n.2576G=
ENST00000532888.6:n.582G=
ENST00000534384.1:n.507G=
ENST00000538950.5:c.68G=	ENSP00000475991.2:p.Trp23=
ENST00000545985.5:c.287G=	ENSP00000475241.2:p.Trp96=
NM_001164277.1:c.287G= , LRG_187t1:c.287G=	NP_001157749.1:p.Trp96=
NM_001164278.1:c.287G=	NP_001157750.1:p.Trp96=
NM_001164279.1:c.68G=	NP_001157751.1:p.Trp23=
NM_001164280.1:c.287G=	NP_001157752.1:p.Trp96=
NM_001467.5:c.287G=	NP_001458.1:p.Trp96=
NM_001164278.2:c.287G=	NP_001157750.1:p.Trp96=
NM_001164279.2:c.68G=	NP_001157751.1:p.Trp23=
NM_001164280.2:c.287G=	NP_001157752.1:p.Trp96=
NM_001467.6:c.287G=	NP_001458.1:p.Trp96=
NM_001164277.2:c.287G= MANE Select	NP_001157749.1:p.Trp96=