Canonical Allele Identifier: CA2003749142

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026640A= , CM000673.2:g.119026640A=	GRCh38
NC_000011.9:g.118897350A= , CM000673.1:g.118897350A=	GRCh37
NC_000011.8:g.118402560A=	NCBI36
NG_013331.1:g.9266T= , LRG_187:g.9266T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.1014+297T=
ENST00000697845.1:n.1235T=
ENST00000697846.1:n.1014+297T=
ENST00000697847.1:n.1063T=
ENST00000697848.1:n.1063T=
ENST00000697849.1:n.2350T=
ENST00000697850.1:n.1063T=
ENST00000697851.1:n.2671T=
ENST00000638186.1:n.1137T=
ENST00000638360.1:n.969T=
ENST00000638925.1:n.1070T=
ENST00000650539.1:n.1239T=
ENST00000330775.9:c.833T=	ENSP00000476242.2:p.Ile278=
ENST00000357590.9:c.833T=	ENSP00000476176.2:p.Ile278=
ENST00000524428.5:n.1106+297T=
ENST00000525039.5:n.1257T=
ENST00000525102.5:n.1591T=
ENST00000525372.5:n.834T=
ENST00000526275.5:n.1615T=
ENST00000527992.5:n.1061T=
ENST00000529510.5:n.558+297T=
ENST00000530407.5:n.983T=
ENST00000532085.1:n.3692T=
ENST00000538950.5:c.614T=	ENSP00000475991.2:p.Ile205=
ENST00000545985.5:c.833T=	ENSP00000475241.2:p.Ile278=
NM_001164277.1:c.833T= , LRG_187t1:c.833T=	NP_001157749.1:p.Ile278=
NM_001164278.1:c.833T=	NP_001157750.1:p.Ile278=
NM_001164279.1:c.614T=	NP_001157751.1:p.Ile205=
NM_001164280.1:c.833T=	NP_001157752.1:p.Ile278=
NM_001467.5:c.833T=	NP_001458.1:p.Ile278=
NM_001164278.2:c.833T=	NP_001157750.1:p.Ile278=
NM_001164279.2:c.614T=	NP_001157751.1:p.Ile205=
NM_001164280.2:c.833T=	NP_001157752.1:p.Ile278=
NM_001467.6:c.833T=	NP_001458.1:p.Ile278=
NM_001164277.2:c.833T= MANE Select	NP_001157749.1:p.Ile278=