Canonical Allele Identifier: CA2003750003

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119028307C= , CM000673.2:g.119028307C=	GRCh38
NC_000011.9:g.118899017C= , CM000673.1:g.118899017C=	GRCh37
NC_000011.8:g.118404227C=	NCBI36
NG_013331.1:g.7600G= , LRG_187:g.7600G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.497G=
ENST00000697845.1:n.421G=
ENST00000697846.1:n.497G=
ENST00000697847.1:n.497G=
ENST00000697848.1:n.497G=
ENST00000697849.1:n.1536G=
ENST00000697850.1:n.497G=
ENST00000697851.1:n.1536G=
ENST00000638186.1:n.571G=
ENST00000638360.1:n.505G=
ENST00000638925.1:n.504G=
ENST00000650539.1:n.673G=
ENST00000330775.9:c.268G=	ENSP00000476242.2:p.Val90=
ENST00000357590.9:c.268G=	ENSP00000476176.2:p.Val90=
ENST00000524428.5:n.268G=
ENST00000525039.5:n.691G=
ENST00000525102.5:n.1025G=
ENST00000525372.5:n.268G=
ENST00000525787.1:n.563G=
ENST00000526275.5:n.728G=
ENST00000526626.6:n.344-435G=
ENST00000527992.5:n.495G=
ENST00000529510.5:n.286G=
ENST00000530407.5:n.417G=
ENST00000532085.1:n.2557G=
ENST00000532888.6:n.563G=
ENST00000534384.1:n.488G=
ENST00000538950.5:c.49G=	ENSP00000475991.2:p.Val17=
ENST00000545985.5:c.268G=	ENSP00000475241.2:p.Val90=
NM_001164277.1:c.268G= , LRG_187t1:c.268G=	NP_001157749.1:p.Val90=
NM_001164278.1:c.268G=	NP_001157750.1:p.Val90=
NM_001164279.1:c.49G=	NP_001157751.1:p.Val17=
NM_001164280.1:c.268G=	NP_001157752.1:p.Val90=
NM_001467.5:c.268G=	NP_001458.1:p.Val90=
NM_001164278.2:c.268G=	NP_001157750.1:p.Val90=
NM_001164279.2:c.49G=	NP_001157751.1:p.Val17=
NM_001164280.2:c.268G=	NP_001157752.1:p.Val90=
NM_001467.6:c.268G=	NP_001458.1:p.Val90=
NM_001164277.2:c.268G= MANE Select	NP_001157749.1:p.Val90=