Canonical Allele Identifier: CA2003749441

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027221G= , CM000673.2:g.119027221G=	GRCh38
NC_000011.9:g.118897931G= , CM000673.1:g.118897931G=	GRCh37
NC_000011.8:g.118403141G=	NCBI36
NG_013331.1:g.8685C= , LRG_187:g.8685C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.856-126C=
ENST00000697845.1:n.780-126C=
ENST00000697846.1:n.856-126C=
ENST00000697847.1:n.856-126C=
ENST00000697848.1:n.856-126C=
ENST00000697849.1:n.1895-126C=
ENST00000697850.1:n.856-126C=
ENST00000697851.1:n.2216-126C=
ENST00000638186.1:n.930-126C=
ENST00000638360.1:n.762-126C=
ENST00000638925.1:n.863-126C=
ENST00000650539.1:n.1032-126C=
ENST00000330775.9:c.626-126C=	ENSP00000476242.2:n.626-126C=
ENST00000357590.9:c.626-126C=	ENSP00000476176.2:n.626-126C=
ENST00000524428.5:n.948-126C=
ENST00000525039.5:n.1050-126C=
ENST00000525102.5:n.1384-126C=
ENST00000525372.5:n.627-126C=
ENST00000526275.5:n.1408-126C=
ENST00000526626.6:n.589-126C=
ENST00000527992.5:n.854-126C=
ENST00000529510.5:n.400-126C=
ENST00000530407.5:n.776-126C=
ENST00000532085.1:n.3237-126C=
ENST00000532888.6:n.922-126C=
ENST00000538950.5:c.407-126C=	ENSP00000475991.2:n.407-126C=
ENST00000545985.5:c.626-126C=	ENSP00000475241.2:n.626-126C=
NM_001164277.1:c.626-126C= , LRG_187t1:c.626-126C=	NP_001157749.1:n.626-126C=
NM_001164278.1:c.626-126C=	NP_001157750.1:n.626-126C=
NM_001164279.1:c.407-126C=	NP_001157751.1:n.407-126C=
NM_001164280.1:c.626-126C=	NP_001157752.1:n.626-126C=
NM_001467.5:c.626-126C=	NP_001458.1:n.626-126C=
NM_001164278.2:c.626-126C=	NP_001157750.1:n.626-126C=
NM_001164279.2:c.407-126C=	NP_001157751.1:n.407-126C=
NM_001164280.2:c.626-126C=	NP_001157752.1:n.626-126C=
NM_001467.6:c.626-126C=	NP_001458.1:n.626-126C=
NM_001164277.2:c.626-126C= MANE Select	NP_001157749.1:n.626-126C=