Canonical Allele Identifier: CA2003775518

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029485A= , CM000673.2:g.119029485A=	GRCh38
NC_000011.9:g.118900195A= , CM000673.1:g.118900195A=	GRCh37
NC_000011.8:g.118405405A=	NCBI36
NG_013331.1:g.6422T= , LRG_187:g.6422T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.114T=
ENST00000697846.1:n.114T=
ENST00000697847.1:n.114T=
ENST00000697848.1:n.114T=
ENST00000697849.1:n.358T=
ENST00000697850.1:n.114T=
ENST00000697851.1:n.358T=
ENST00000638186.1:n.188T=
ENST00000638360.1:n.122T=
ENST00000638925.1:n.121T=
ENST00000650539.1:n.290T=
ENST00000330775.9:c.-116T=	ENSP00000476242.2:n.-116T=
ENST00000357590.9:c.-116T=	ENSP00000476176.2:n.-116T=
ENST00000525039.5:n.308T=
ENST00000525102.5:n.642T=
ENST00000525787.1:n.180T=
ENST00000526626.6:n.80T=
ENST00000527992.5:n.112T=
ENST00000530407.5:n.104T=
ENST00000532085.1:n.1379T=
ENST00000532888.6:n.80T=
ENST00000534384.1:n.105T=
ENST00000538950.5:c.-265T=	ENSP00000475991.2:n.-265T=
ENST00000545985.5:c.-116T=	ENSP00000475241.2:n.-116T=
NM_001164277.1:c.-116T= , LRG_187t1:c.-116T=	NP_001157749.1:n.-116T=
NM_001164278.1:c.-116T=	NP_001157750.1:n.-116T=
NM_001164279.1:c.-265T=	NP_001157751.1:n.-265T=
NM_001164280.1:c.-116T=	NP_001157752.1:n.-116T=
NM_001467.5:c.-116T=	NP_001458.1:n.-116T=
NM_001164278.2:c.-116T=	NP_001157750.1:n.-116T=
NM_001164279.2:c.-265T=	NP_001157751.1:n.-265T=
NM_001467.6:c.-116T=	NP_001458.1:n.-116T=
NM_001164277.2:c.-116T= MANE Select	NP_001157749.1:n.-116T=