Canonical Allele Identifier: CA2003775296

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029371G= , CM000673.2:g.119029371G=	GRCh38
NC_000011.9:g.118900081G= , CM000673.1:g.118900081G=	GRCh37
NC_000011.8:g.118405291G=	NCBI36
NG_013331.1:g.6536C= , LRG_187:g.6536C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.228C=
ENST00000697846.1:n.228C=
ENST00000697847.1:n.228C=
ENST00000697848.1:n.228C=
ENST00000697849.1:n.472C=
ENST00000697850.1:n.228C=
ENST00000697851.1:n.472C=
ENST00000638186.1:n.302C=
ENST00000638360.1:n.236C=
ENST00000638925.1:n.235C=
ENST00000650539.1:n.404C=
ENST00000330775.9:c.-2C=	ENSP00000476242.2:n.-2C=
ENST00000357590.9:c.-2C=	ENSP00000476176.2:n.-2C=
ENST00000525039.5:n.422C=
ENST00000525102.5:n.756C=
ENST00000525787.1:n.294C=
ENST00000526626.6:n.194C=
ENST00000527992.5:n.226C=
ENST00000529510.5:n.17C=
ENST00000530407.5:n.197+21C=
ENST00000532085.1:n.1493C=
ENST00000532888.6:n.194C=
ENST00000534384.1:n.219C=
ENST00000538950.5:c.-172+21C=	ENSP00000475991.2:n.-172+21C=
ENST00000545985.5:c.-2C=	ENSP00000475241.2:n.-2C=
NM_001164277.1:c.-2C= , LRG_187t1:c.-2C=	NP_001157749.1:n.-2C=
NM_001164278.1:c.-2C=	NP_001157750.1:n.-2C=
NM_001164279.1:c.-172+21C=	NP_001157751.1:n.-172+21C=
NM_001164280.1:c.-2C=	NP_001157752.1:n.-2C=
NM_001467.5:c.-2C=	NP_001458.1:n.-2C=
NM_001164278.2:c.-2C=	NP_001157750.1:n.-2C=
NM_001164279.2:c.-172+21C=	NP_001157751.1:n.-172+21C=
NM_001164280.2:c.-2C=	NP_001157752.1:n.-2C=
NM_001467.6:c.-2C=	NP_001458.1:n.-2C=
NM_001164277.2:c.-2C= MANE Select	NP_001157749.1:n.-2C=