Canonical Allele Identifier: CA2003748592

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025582T= , CM000673.2:g.119025582T=	GRCh38
NC_000011.9:g.118896292T= , CM000673.1:g.118896292T=	GRCh37
NC_000011.8:g.118401502T=	NCBI36
NG_013331.1:g.10324A= , LRG_187:g.10324A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1194+110A=
ENST00000697845.1:n.2183+110A=
ENST00000697846.1:n.1304A=
ENST00000697847.1:n.1267+110A=
ENST00000697848.1:n.1390A=
ENST00000697849.1:n.3408A=
ENST00000697850.1:n.1599A=
ENST00000697851.1:n.2823-253A=
ENST00000638186.1:n.1289-253A=
ENST00000638360.1:n.1121-253A=
ENST00000638925.1:n.1254-253A=
ENST00000650539.1:n.1456+110A=
ENST00000330775.9:c.985-253A=	ENSP00000476242.2:n.985-253A=
ENST00000357590.9:c.1050+110A=	ENSP00000476176.2:n.1050+110A=
ENST00000524428.5:n.1221-253A=
ENST00000525039.5:n.1474+110A=
ENST00000525102.5:n.1743-253A=
ENST00000525372.5:n.1083-253A=
ENST00000526275.5:n.1767-253A=
ENST00000527992.5:n.1213-253A=
ENST00000529510.5:n.673-253A=
ENST00000530407.5:n.1135-253A=
ENST00000532085.1:n.4750A=
ENST00000538950.5:c.766-253A=	ENSP00000475991.2:n.766-253A=
ENST00000545985.5:c.985-253A=	ENSP00000475241.2:n.985-253A=
NM_001164277.1:c.985-253A= , LRG_187t1:c.985-253A=	NP_001157749.1:n.985-253A=
NM_001164278.1:c.1050+110A=	NP_001157750.1:n.1050+110A=
NM_001164279.1:c.766-253A=	NP_001157751.1:n.766-253A=
NM_001164280.1:c.985-253A=	NP_001157752.1:n.985-253A=
NM_001467.5:c.985-253A=	NP_001458.1:n.985-253A=
NM_001164278.2:c.1050+110A=	NP_001157750.1:n.1050+110A=
NM_001164279.2:c.766-253A=	NP_001157751.1:n.766-253A=
NM_001164280.2:c.985-253A=	NP_001157752.1:n.985-253A=
NM_001467.6:c.985-253A=	NP_001458.1:n.985-253A=
NM_001164277.2:c.985-253A= MANE Select	NP_001157749.1:n.985-253A=