Canonical Allele Identifier: CA2003775500

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029478C= , CM000673.2:g.119029478C=	GRCh38
NC_000011.9:g.118900188C= , CM000673.1:g.118900188C=	GRCh37
NC_000011.8:g.118405398C=	NCBI36
NG_013331.1:g.6429G= , LRG_187:g.6429G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.121G=
ENST00000697846.1:n.121G=
ENST00000697847.1:n.121G=
ENST00000697848.1:n.121G=
ENST00000697849.1:n.365G=
ENST00000697850.1:n.121G=
ENST00000697851.1:n.365G=
ENST00000638186.1:n.195G=
ENST00000638360.1:n.129G=
ENST00000638925.1:n.128G=
ENST00000650539.1:n.297G=
ENST00000330775.9:c.-109G=	ENSP00000476242.2:n.-109G=
ENST00000357590.9:c.-109G=	ENSP00000476176.2:n.-109G=
ENST00000525039.5:n.315G=
ENST00000525102.5:n.649G=
ENST00000525787.1:n.187G=
ENST00000526626.6:n.87G=
ENST00000527992.5:n.119G=
ENST00000530407.5:n.111G=
ENST00000532085.1:n.1386G=
ENST00000532888.6:n.87G=
ENST00000534384.1:n.112G=
ENST00000538950.5:c.-258G=	ENSP00000475991.2:n.-258G=
ENST00000545985.5:c.-109G=	ENSP00000475241.2:n.-109G=
NM_001164277.1:c.-109G= , LRG_187t1:c.-109G=	NP_001157749.1:n.-109G=
NM_001164278.1:c.-109G=	NP_001157750.1:n.-109G=
NM_001164279.1:c.-258G=	NP_001157751.1:n.-258G=
NM_001164280.1:c.-109G=	NP_001157752.1:n.-109G=
NM_001467.5:c.-109G=	NP_001458.1:n.-109G=
NM_001164278.2:c.-109G=	NP_001157750.1:n.-109G=
NM_001164279.2:c.-258G=	NP_001157751.1:n.-258G=
NM_001164280.2:c.-109G=	NP_001157752.1:n.-109G=
NM_001467.6:c.-109G=	NP_001458.1:n.-109G=
NM_001164277.2:c.-109G= MANE Select	NP_001157749.1:n.-109G=