Canonical Allele Identifier: CA2003775291

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029370G= , CM000673.2:g.119029370G=	GRCh38
NC_000011.9:g.118900080G= , CM000673.1:g.118900080G=	GRCh37
NC_000011.8:g.118405290G=	NCBI36
NG_013331.1:g.6537C= , LRG_187:g.6537C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.229C=
ENST00000697846.1:n.229C=
ENST00000697847.1:n.229C=
ENST00000697848.1:n.229C=
ENST00000697849.1:n.473C=
ENST00000697850.1:n.229C=
ENST00000697851.1:n.473C=
ENST00000638186.1:n.303C=
ENST00000638360.1:n.237C=
ENST00000638925.1:n.236C=
ENST00000650539.1:n.405C=
ENST00000330775.9:c.-1C=	ENSP00000476242.2:n.-1C=
ENST00000357590.9:c.-1C=	ENSP00000476176.2:n.-1C=
ENST00000525039.5:n.423C=
ENST00000525102.5:n.757C=
ENST00000525787.1:n.295C=
ENST00000526626.6:n.195C=
ENST00000527992.5:n.227C=
ENST00000529510.5:n.18C=
ENST00000530407.5:n.197+22C=
ENST00000532085.1:n.1494C=
ENST00000532888.6:n.195C=
ENST00000534384.1:n.220C=
ENST00000538950.5:c.-172+22C=	ENSP00000475991.2:n.-172+22C=
ENST00000545985.5:c.-1C=	ENSP00000475241.2:n.-1C=
NM_001164277.1:c.-1C= , LRG_187t1:c.-1C=	NP_001157749.1:n.-1C=
NM_001164278.1:c.-1C=	NP_001157750.1:n.-1C=
NM_001164279.1:c.-172+22C=	NP_001157751.1:n.-172+22C=
NM_001164280.1:c.-1C=	NP_001157752.1:n.-1C=
NM_001467.5:c.-1C=	NP_001458.1:n.-1C=
NM_001164278.2:c.-1C=	NP_001157750.1:n.-1C=
NM_001164279.2:c.-172+22C=	NP_001157751.1:n.-172+22C=
NM_001164280.2:c.-1C=	NP_001157752.1:n.-1C=
NM_001467.6:c.-1C=	NP_001458.1:n.-1C=
NM_001164277.2:c.-1C= MANE Select	NP_001157749.1:n.-1C=