Canonical Allele Identifier: CA2003775360

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029397A= , CM000673.2:g.119029397A=	GRCh38
NC_000011.9:g.118900107A= , CM000673.1:g.118900107A=	GRCh37
NC_000011.8:g.118405317A=	NCBI36
NG_013331.1:g.6510T= , LRG_187:g.6510T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.202T=
ENST00000697846.1:n.202T=
ENST00000697847.1:n.202T=
ENST00000697848.1:n.202T=
ENST00000697849.1:n.446T=
ENST00000697850.1:n.202T=
ENST00000697851.1:n.446T=
ENST00000638186.1:n.276T=
ENST00000638360.1:n.210T=
ENST00000638925.1:n.209T=
ENST00000650539.1:n.378T=
ENST00000330775.9:c.-28T=	ENSP00000476242.2:n.-28T=
ENST00000357590.9:c.-28T=	ENSP00000476176.2:n.-28T=
ENST00000525039.5:n.396T=
ENST00000525102.5:n.730T=
ENST00000525787.1:n.268T=
ENST00000526626.6:n.168T=
ENST00000527992.5:n.200T=
ENST00000530407.5:n.192T=
ENST00000532085.1:n.1467T=
ENST00000532888.6:n.168T=
ENST00000534384.1:n.193T=
ENST00000538950.5:c.-177T=	ENSP00000475991.2:n.-177T=
ENST00000545985.5:c.-28T=	ENSP00000475241.2:n.-28T=
NM_001164277.1:c.-28T= , LRG_187t1:c.-28T=	NP_001157749.1:n.-28T=
NM_001164278.1:c.-28T=	NP_001157750.1:n.-28T=
NM_001164279.1:c.-177T=	NP_001157751.1:n.-177T=
NM_001164280.1:c.-28T=	NP_001157752.1:n.-28T=
NM_001467.5:c.-28T=	NP_001458.1:n.-28T=
NM_001164278.2:c.-28T=	NP_001157750.1:n.-28T=
NM_001164279.2:c.-177T=	NP_001157751.1:n.-177T=
NM_001164280.2:c.-28T=	NP_001157752.1:n.-28T=
NM_001467.6:c.-28T=	NP_001458.1:n.-28T=
NM_001164277.2:c.-28T= MANE Select	NP_001157749.1:n.-28T=