Canonical Allele Identifier: CA2003748824

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025997G= , CM000673.2:g.119025997G=	GRCh38
NC_000011.9:g.118896707G= , CM000673.1:g.118896707G=	GRCh37
NC_000011.8:g.118401917G=	NCBI36
NG_013331.1:g.9909C= , LRG_187:g.9909C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1098C=
ENST00000697845.1:n.1878C=
ENST00000697846.1:n.1098C=
ENST00000697847.1:n.1202-240C=
ENST00000697848.1:n.1184C=
ENST00000697849.1:n.2993C=
ENST00000697850.1:n.1184C=
ENST00000697851.1:n.2792C=
ENST00000638186.1:n.1258C=
ENST00000638360.1:n.1090C=
ENST00000638925.1:n.1223C=
ENST00000650539.1:n.1360C=
ENST00000330775.9:c.954C=	ENSP00000476242.2:p.Phe318=
ENST00000357590.9:c.954C=	ENSP00000476176.2:p.Phe318=
ENST00000524428.5:n.1190C=
ENST00000525039.5:n.1378C=
ENST00000525102.5:n.1712C=
ENST00000525372.5:n.1052C=
ENST00000526275.5:n.1736C=
ENST00000527992.5:n.1182C=
ENST00000529510.5:n.642C=
ENST00000530407.5:n.1104C=
ENST00000532085.1:n.4335C=
ENST00000538950.5:c.735C=	ENSP00000475991.2:p.Phe245=
ENST00000545985.5:c.954C=	ENSP00000475241.2:p.Phe318=
NM_001164277.1:c.954C= , LRG_187t1:c.954C=	NP_001157749.1:p.Phe318=
NM_001164278.1:c.954C=	NP_001157750.1:p.Phe318=
NM_001164279.1:c.735C=	NP_001157751.1:p.Phe245=
NM_001164280.1:c.954C=	NP_001157752.1:p.Phe318=
NM_001467.5:c.954C=	NP_001458.1:p.Phe318=
NM_001164278.2:c.954C=	NP_001157750.1:p.Phe318=
NM_001164279.2:c.735C=	NP_001157751.1:p.Phe245=
NM_001164280.2:c.954C=	NP_001157752.1:p.Phe318=
NM_001467.6:c.954C=	NP_001458.1:p.Phe318=
NM_001164277.2:c.954C= MANE Select	NP_001157749.1:p.Phe318=