Canonical Allele Identifier: CA2003749770

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027863G= , CM000673.2:g.119027863G=	GRCh38
NC_000011.9:g.118898573G= , CM000673.1:g.118898573G=	GRCh37
NC_000011.8:g.118403783G=	NCBI36
NG_013331.1:g.8044C= , LRG_187:g.8044C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.620C=
ENST00000697845.1:n.544C=
ENST00000697846.1:n.620C=
ENST00000697847.1:n.620C=
ENST00000697848.1:n.620C=
ENST00000697849.1:n.1659C=
ENST00000697850.1:n.620C=
ENST00000697851.1:n.1980C=
ENST00000638186.1:n.694C=
ENST00000638360.1:n.619-93C=
ENST00000638925.1:n.627C=
ENST00000650539.1:n.796C=
ENST00000330775.9:c.391C=	ENSP00000476242.2:p.Pro131=
ENST00000357590.9:c.391C=	ENSP00000476176.2:p.Pro131=
ENST00000524428.5:n.712C=
ENST00000525039.5:n.814C=
ENST00000525102.5:n.1148C=
ENST00000525372.5:n.391C=
ENST00000525787.1:n.1007C=
ENST00000526275.5:n.1172C=
ENST00000526626.6:n.353C=
ENST00000527992.5:n.618C=
ENST00000529510.5:n.399+331C=
ENST00000530407.5:n.540C=
ENST00000532085.1:n.3001C=
ENST00000532888.6:n.686C=
ENST00000538950.5:c.172C=	ENSP00000475991.2:p.Pro58=
ENST00000545985.5:c.391C=	ENSP00000475241.2:p.Pro131=
NM_001164277.1:c.391C= , LRG_187t1:c.391C=	NP_001157749.1:p.Pro131=
NM_001164278.1:c.391C=	NP_001157750.1:p.Pro131=
NM_001164279.1:c.172C=	NP_001157751.1:p.Pro58=
NM_001164280.1:c.391C=	NP_001157752.1:p.Pro131=
NM_001467.5:c.391C=	NP_001458.1:p.Pro131=
NM_001164278.2:c.391C=	NP_001157750.1:p.Pro131=
NM_001164279.2:c.172C=	NP_001157751.1:p.Pro58=
NM_001164280.2:c.391C=	NP_001157752.1:p.Pro131=
NM_001467.6:c.391C=	NP_001458.1:p.Pro131=
NM_001164277.2:c.391C= MANE Select	NP_001157749.1:p.Pro131=