Canonical Allele Identifier: CA2003775200

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029342G= , CM000673.2:g.119029342G=	GRCh38
NC_000011.9:g.118900052G= , CM000673.1:g.118900052G=	GRCh37
NC_000011.8:g.118405262G=	NCBI36
NG_013331.1:g.6565C= , LRG_187:g.6565C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.257C=
ENST00000697846.1:n.257C=
ENST00000697847.1:n.257C=
ENST00000697848.1:n.257C=
ENST00000697849.1:n.501C=
ENST00000697850.1:n.257C=
ENST00000697851.1:n.501C=
ENST00000638186.1:n.331C=
ENST00000638360.1:n.265C=
ENST00000638925.1:n.264C=
ENST00000650539.1:n.433C=
ENST00000330775.9:c.28C=	ENSP00000476242.2:p.Arg10=
ENST00000357590.9:c.28C=	ENSP00000476176.2:p.Arg10=
ENST00000524428.5:n.28C=
ENST00000525039.5:n.451C=
ENST00000525102.5:n.785C=
ENST00000525372.5:n.28C=
ENST00000525787.1:n.323C=
ENST00000526626.6:n.223C=
ENST00000527992.5:n.255C=
ENST00000529510.5:n.46C=
ENST00000530407.5:n.197+50C=
ENST00000532085.1:n.1522C=
ENST00000532888.6:n.223C=
ENST00000534384.1:n.248C=
ENST00000538950.5:c.-172+50C=	ENSP00000475991.2:n.-172+50C=
ENST00000545985.5:c.28C=	ENSP00000475241.2:p.Arg10=
NM_001164277.1:c.28C= , LRG_187t1:c.28C=	NP_001157749.1:p.Arg10=
NM_001164278.1:c.28C=	NP_001157750.1:p.Arg10=
NM_001164279.1:c.-172+50C=	NP_001157751.1:n.-172+50C=
NM_001164280.1:c.28C=	NP_001157752.1:p.Arg10=
NM_001467.5:c.28C=	NP_001458.1:p.Arg10=
NM_001164278.2:c.28C=	NP_001157750.1:p.Arg10=
NM_001164279.2:c.-172+50C=	NP_001157751.1:n.-172+50C=
NM_001164280.2:c.28C=	NP_001157752.1:p.Arg10=
NM_001467.6:c.28C=	NP_001458.1:p.Arg10=
NM_001164277.2:c.28C= MANE Select	NP_001157749.1:p.Arg10=