Canonical Allele Identifier: CA2003749693

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027722C= , CM000673.2:g.119027722C=	GRCh38
NC_000011.9:g.118898432C= , CM000673.1:g.118898432C=	GRCh37
NC_000011.8:g.118403642C=	NCBI36
NG_013331.1:g.8184G= , LRG_187:g.8184G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.761G=
ENST00000697845.1:n.685G=
ENST00000697846.1:n.761G=
ENST00000697847.1:n.761G=
ENST00000697848.1:n.761G=
ENST00000697849.1:n.1800G=
ENST00000697850.1:n.761G=
ENST00000697851.1:n.2121G=
ENST00000638186.1:n.835G=
ENST00000638360.1:n.667G=
ENST00000638925.1:n.768G=
ENST00000650539.1:n.937G=
ENST00000330775.9:c.531G=	ENSP00000476242.2:p.Val177=
ENST00000357590.9:c.531G=	ENSP00000476176.2:p.Val177=
ENST00000524428.5:n.853G=
ENST00000525039.5:n.955G=
ENST00000525102.5:n.1289G=
ENST00000525372.5:n.532G=
ENST00000526275.5:n.1313G=
ENST00000526626.6:n.494G=
ENST00000527992.5:n.759G=
ENST00000529510.5:n.399+472G=
ENST00000530407.5:n.681G=
ENST00000532085.1:n.3142G=
ENST00000532888.6:n.827G=
ENST00000538950.5:c.312G=	ENSP00000475991.2:p.Val104=
ENST00000545985.5:c.531G=	ENSP00000475241.2:p.Val177=
NM_001164277.1:c.531G= , LRG_187t1:c.531G=	NP_001157749.1:p.Val177=
NM_001164278.1:c.531G=	NP_001157750.1:p.Val177=
NM_001164279.1:c.312G=	NP_001157751.1:p.Val104=
NM_001164280.1:c.531G=	NP_001157752.1:p.Val177=
NM_001467.5:c.531G=	NP_001458.1:p.Val177=
NM_001164278.2:c.531G=	NP_001157750.1:p.Val177=
NM_001164279.2:c.312G=	NP_001157751.1:p.Val104=
NM_001164280.2:c.531G=	NP_001157752.1:p.Val177=
NM_001467.6:c.531G=	NP_001458.1:p.Val177=
NM_001164277.2:c.531G= MANE Select	NP_001157749.1:p.Val177=