Canonical Allele Identifier: CA2003775328

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029385G= , CM000673.2:g.119029385G=	GRCh38
NC_000011.9:g.118900095G= , CM000673.1:g.118900095G=	GRCh37
NC_000011.8:g.118405305G=	NCBI36
NG_013331.1:g.6522C= , LRG_187:g.6522C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.214C=
ENST00000697846.1:n.214C=
ENST00000697847.1:n.214C=
ENST00000697848.1:n.214C=
ENST00000697849.1:n.458C=
ENST00000697850.1:n.214C=
ENST00000697851.1:n.458C=
ENST00000638186.1:n.288C=
ENST00000638360.1:n.222C=
ENST00000638925.1:n.221C=
ENST00000650539.1:n.390C=
ENST00000330775.9:c.-16C=	ENSP00000476242.2:n.-16C=
ENST00000357590.9:c.-16C=	ENSP00000476176.2:n.-16C=
ENST00000525039.5:n.408C=
ENST00000525102.5:n.742C=
ENST00000525787.1:n.280C=
ENST00000526626.6:n.180C=
ENST00000527992.5:n.212C=
ENST00000529510.5:n.3C=
ENST00000530407.5:n.197+7C=
ENST00000532085.1:n.1479C=
ENST00000532888.6:n.180C=
ENST00000534384.1:n.205C=
ENST00000538950.5:c.-172+7C=	ENSP00000475991.2:n.-172+7C=
ENST00000545985.5:c.-16C=	ENSP00000475241.2:n.-16C=
NM_001164277.1:c.-16C= , LRG_187t1:c.-16C=	NP_001157749.1:n.-16C=
NM_001164278.1:c.-16C=	NP_001157750.1:n.-16C=
NM_001164279.1:c.-172+7C=	NP_001157751.1:n.-172+7C=
NM_001164280.1:c.-16C=	NP_001157752.1:n.-16C=
NM_001467.5:c.-16C=	NP_001458.1:n.-16C=
NM_001164278.2:c.-16C=	NP_001157750.1:n.-16C=
NM_001164279.2:c.-172+7C=	NP_001157751.1:n.-172+7C=
NM_001164280.2:c.-16C=	NP_001157752.1:n.-16C=
NM_001467.6:c.-16C=	NP_001458.1:n.-16C=
NM_001164277.2:c.-16C= MANE Select	NP_001157749.1:n.-16C=