Canonical Allele Identifier: CA2003749183

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026716G= , CM000673.2:g.119026716G=	GRCh38
NC_000011.9:g.118897426G= , CM000673.1:g.118897426G=	GRCh37
NC_000011.8:g.118402636G=	NCBI36
NG_013331.1:g.9190C= , LRG_187:g.9190C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1014+221C=
ENST00000697845.1:n.1159C=
ENST00000697846.1:n.1014+221C=
ENST00000697847.1:n.1015-28C=
ENST00000697848.1:n.1015-28C=
ENST00000697849.1:n.2274C=
ENST00000697850.1:n.1015-28C=
ENST00000697851.1:n.2595C=
ENST00000638186.1:n.1089-28C=
ENST00000638360.1:n.921-28C=
ENST00000638925.1:n.1022-28C=
ENST00000650539.1:n.1191-28C=
ENST00000330775.9:c.785-28C=	ENSP00000476242.2:n.785-28C=
ENST00000357590.9:c.785-28C=	ENSP00000476176.2:n.785-28C=
ENST00000524428.5:n.1106+221C=
ENST00000525039.5:n.1209-28C=
ENST00000525102.5:n.1543-28C=
ENST00000525372.5:n.786-28C=
ENST00000526275.5:n.1567-28C=
ENST00000527992.5:n.1013-28C=
ENST00000529510.5:n.558+221C=
ENST00000530407.5:n.935-28C=
ENST00000532085.1:n.3616C=
ENST00000532888.6:n.1301C=
ENST00000538950.5:c.566-28C=	ENSP00000475991.2:n.566-28C=
ENST00000545985.5:c.785-28C=	ENSP00000475241.2:n.785-28C=
NM_001164277.1:c.785-28C= , LRG_187t1:c.785-28C=	NP_001157749.1:n.785-28C=
NM_001164278.1:c.785-28C=	NP_001157750.1:n.785-28C=
NM_001164279.1:c.566-28C=	NP_001157751.1:n.566-28C=
NM_001164280.1:c.785-28C=	NP_001157752.1:n.785-28C=
NM_001467.5:c.785-28C=	NP_001458.1:n.785-28C=
NM_001164278.2:c.785-28C=	NP_001157750.1:n.785-28C=
NM_001164279.2:c.566-28C=	NP_001157751.1:n.566-28C=
NM_001164280.2:c.785-28C=	NP_001157752.1:n.785-28C=
NM_001467.6:c.785-28C=	NP_001458.1:n.785-28C=
NM_001164277.2:c.785-28C= MANE Select	NP_001157749.1:n.785-28C=