Canonical Allele Identifier: CA2003749354

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027048A= , CM000673.2:g.119027048A=	GRCh38
NC_000011.9:g.118897758A= , CM000673.1:g.118897758A=	GRCh37
NC_000011.8:g.118402968A=	NCBI36
NG_013331.1:g.8858T= , LRG_187:g.8858T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.903T=
ENST00000697845.1:n.827T=
ENST00000697846.1:n.903T=
ENST00000697847.1:n.903T=
ENST00000697848.1:n.903T=
ENST00000697849.1:n.1942T=
ENST00000697850.1:n.903T=
ENST00000697851.1:n.2263T=
ENST00000638186.1:n.977T=
ENST00000638360.1:n.809T=
ENST00000638925.1:n.910T=
ENST00000650539.1:n.1079T=
ENST00000330775.9:c.673T=	ENSP00000476242.2:p.Tyr225=
ENST00000357590.9:c.673T=	ENSP00000476176.2:p.Tyr225=
ENST00000524428.5:n.995T=
ENST00000525039.5:n.1097T=
ENST00000525102.5:n.1431T=
ENST00000525372.5:n.674T=
ENST00000526275.5:n.1455T=
ENST00000526626.6:n.636T=
ENST00000527992.5:n.901T=
ENST00000529510.5:n.447T=
ENST00000530407.5:n.823T=
ENST00000532085.1:n.3284T=
ENST00000532888.6:n.969T=
ENST00000538950.5:c.454T=	ENSP00000475991.2:p.Tyr152=
ENST00000545985.5:c.673T=	ENSP00000475241.2:p.Tyr225=
NM_001164277.1:c.673T= , LRG_187t1:c.673T=	NP_001157749.1:p.Tyr225=
NM_001164278.1:c.673T=	NP_001157750.1:p.Tyr225=
NM_001164279.1:c.454T=	NP_001157751.1:p.Tyr152=
NM_001164280.1:c.673T=	NP_001157752.1:p.Tyr225=
NM_001467.5:c.673T=	NP_001458.1:p.Tyr225=
NM_001164278.2:c.673T=	NP_001157750.1:p.Tyr225=
NM_001164279.2:c.454T=	NP_001157751.1:p.Tyr152=
NM_001164280.2:c.673T=	NP_001157752.1:p.Tyr225=
NM_001467.6:c.673T=	NP_001458.1:p.Tyr225=
NM_001164277.2:c.673T= MANE Select	NP_001157749.1:p.Tyr225=