Canonical Allele Identifier: CA2003749483

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027293G= , CM000673.2:g.119027293G=	GRCh38
NC_000011.9:g.118898003G= , CM000673.1:g.118898003G=	GRCh37
NC_000011.8:g.118403213G=	NCBI36
NG_013331.1:g.8613C= , LRG_187:g.8613C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.856-198C=
ENST00000697845.1:n.780-198C=
ENST00000697846.1:n.856-198C=
ENST00000697847.1:n.856-198C=
ENST00000697848.1:n.856-198C=
ENST00000697849.1:n.1895-198C=
ENST00000697850.1:n.856-198C=
ENST00000697851.1:n.2216-198C=
ENST00000638186.1:n.930-198C=
ENST00000638360.1:n.762-198C=
ENST00000638925.1:n.863-198C=
ENST00000650539.1:n.1032-198C=
ENST00000330775.9:c.626-198C=	ENSP00000476242.2:n.626-198C=
ENST00000357590.9:c.626-198C=	ENSP00000476176.2:n.626-198C=
ENST00000524428.5:n.948-198C=
ENST00000525039.5:n.1050-198C=
ENST00000525102.5:n.1384-198C=
ENST00000525372.5:n.627-198C=
ENST00000526275.5:n.1408-198C=
ENST00000526626.6:n.589-198C=
ENST00000527992.5:n.854-198C=
ENST00000529510.5:n.400-198C=
ENST00000530407.5:n.776-198C=
ENST00000532085.1:n.3237-198C=
ENST00000532888.6:n.922-198C=
ENST00000538950.5:c.407-198C=	ENSP00000475991.2:n.407-198C=
ENST00000545985.5:c.626-198C=	ENSP00000475241.2:n.626-198C=
NM_001164277.1:c.626-198C= , LRG_187t1:c.626-198C=	NP_001157749.1:n.626-198C=
NM_001164278.1:c.626-198C=	NP_001157750.1:n.626-198C=
NM_001164279.1:c.407-198C=	NP_001157751.1:n.407-198C=
NM_001164280.1:c.626-198C=	NP_001157752.1:n.626-198C=
NM_001467.5:c.626-198C=	NP_001458.1:n.626-198C=
NM_001164278.2:c.626-198C=	NP_001157750.1:n.626-198C=
NM_001164279.2:c.407-198C=	NP_001157751.1:n.407-198C=
NM_001164280.2:c.626-198C=	NP_001157752.1:n.626-198C=
NM_001467.6:c.626-198C=	NP_001458.1:n.626-198C=
NM_001164277.2:c.626-198C= MANE Select	NP_001157749.1:n.626-198C=