Canonical Allele Identifier: CA2003750001

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119028301T= , CM000673.2:g.119028301T=	GRCh38
NC_000011.9:g.118899011T= , CM000673.1:g.118899011T=	GRCh37
NC_000011.8:g.118404221T=	NCBI36
NG_013331.1:g.7606A= , LRG_187:g.7606A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.503A=
ENST00000697845.1:n.427A=
ENST00000697846.1:n.503A=
ENST00000697847.1:n.503A=
ENST00000697848.1:n.503A=
ENST00000697849.1:n.1542A=
ENST00000697850.1:n.503A=
ENST00000697851.1:n.1542A=
ENST00000638186.1:n.577A=
ENST00000638360.1:n.511A=
ENST00000638925.1:n.510A=
ENST00000650539.1:n.679A=
ENST00000330775.9:c.274A=	ENSP00000476242.2:p.Ile92=
ENST00000357590.9:c.274A=	ENSP00000476176.2:p.Ile92=
ENST00000524428.5:n.274A=
ENST00000525039.5:n.697A=
ENST00000525102.5:n.1031A=
ENST00000525372.5:n.274A=
ENST00000525787.1:n.569A=
ENST00000526275.5:n.734A=
ENST00000526626.6:n.344-429A=
ENST00000527992.5:n.501A=
ENST00000529510.5:n.292A=
ENST00000530407.5:n.423A=
ENST00000532085.1:n.2563A=
ENST00000532888.6:n.569A=
ENST00000534384.1:n.494A=
ENST00000538950.5:c.55A=	ENSP00000475991.2:p.Ile19=
ENST00000545985.5:c.274A=	ENSP00000475241.2:p.Ile92=
NM_001164277.1:c.274A= , LRG_187t1:c.274A=	NP_001157749.1:p.Ile92=
NM_001164278.1:c.274A=	NP_001157750.1:p.Ile92=
NM_001164279.1:c.55A=	NP_001157751.1:p.Ile19=
NM_001164280.1:c.274A=	NP_001157752.1:p.Ile92=
NM_001467.5:c.274A=	NP_001458.1:p.Ile92=
NM_001164278.2:c.274A=	NP_001157750.1:p.Ile92=
NM_001164279.2:c.55A=	NP_001157751.1:p.Ile19=
NM_001164280.2:c.274A=	NP_001157752.1:p.Ile92=
NM_001467.6:c.274A=	NP_001458.1:p.Ile92=
NM_001164277.2:c.274A= MANE Select	NP_001157749.1:p.Ile92=