Canonical Allele Identifier: CA2003750031

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119028369A= , CM000673.2:g.119028369A=	GRCh38
NC_000011.9:g.118899079A= , CM000673.1:g.118899079A=	GRCh37
NC_000011.8:g.118404289A=	NCBI36
NG_013331.1:g.7538T= , LRG_187:g.7538T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.435T=
ENST00000697845.1:n.359T=
ENST00000697846.1:n.435T=
ENST00000697847.1:n.435T=
ENST00000697848.1:n.435T=
ENST00000697849.1:n.1474T=
ENST00000697850.1:n.435T=
ENST00000697851.1:n.1474T=
ENST00000638186.1:n.509T=
ENST00000638360.1:n.443T=
ENST00000638925.1:n.442T=
ENST00000650539.1:n.611T=
ENST00000330775.9:c.206T=	ENSP00000476242.2:p.Val69=
ENST00000357590.9:c.206T=	ENSP00000476176.2:p.Val69=
ENST00000524428.5:n.206T=
ENST00000525039.5:n.629T=
ENST00000525102.5:n.963T=
ENST00000525372.5:n.206T=
ENST00000525787.1:n.501T=
ENST00000526275.5:n.666T=
ENST00000526626.6:n.344-497T=
ENST00000527992.5:n.433T=
ENST00000529510.5:n.224T=
ENST00000530407.5:n.355T=
ENST00000532085.1:n.2495T=
ENST00000532888.6:n.501T=
ENST00000534384.1:n.426T=
ENST00000538950.5:c.-14T=	ENSP00000475991.2:n.-14T=
ENST00000545985.5:c.206T=	ENSP00000475241.2:p.Val69=
NM_001164277.1:c.206T= , LRG_187t1:c.206T=	NP_001157749.1:p.Val69=
NM_001164278.1:c.206T=	NP_001157750.1:p.Val69=
NM_001164279.1:c.-14T=	NP_001157751.1:n.-14T=
NM_001164280.1:c.206T=	NP_001157752.1:p.Val69=
NM_001467.5:c.206T=	NP_001458.1:p.Val69=
NM_001164278.2:c.206T=	NP_001157750.1:p.Val69=
NM_001164279.2:c.-14T=	NP_001157751.1:n.-14T=
NM_001164280.2:c.206T=	NP_001157752.1:p.Val69=
NM_001467.6:c.206T=	NP_001458.1:p.Val69=
NM_001164277.2:c.206T= MANE Select	NP_001157749.1:p.Val69=