Canonical Allele Identifier: CA2003748668

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025742T= , CM000673.2:g.119025742T=	GRCh38
NC_000011.9:g.118896452T= , CM000673.1:g.118896452T=	GRCh37
NC_000011.8:g.118401662T=	NCBI36
NG_013331.1:g.10164A= , LRG_187:g.10164A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1144A=
ENST00000697845.1:n.2133A=
ENST00000697846.1:n.1144A=
ENST00000697847.1:n.1217A=
ENST00000697848.1:n.1230A=
ENST00000697849.1:n.3248A=
ENST00000697850.1:n.1439A=
ENST00000697851.1:n.2822+225A=
ENST00000638186.1:n.1288+225A=
ENST00000638360.1:n.1120+225A=
ENST00000638925.1:n.1253+225A=
ENST00000650539.1:n.1406A=
ENST00000330775.9:c.984+225A=	ENSP00000476242.2:n.984+225A=
ENST00000357590.9:c.1000A=	ENSP00000476176.2:p.Thr334=
ENST00000524428.5:n.1220+225A=
ENST00000525039.5:n.1424A=
ENST00000525102.5:n.1742+225A=
ENST00000525372.5:n.1082+225A=
ENST00000526275.5:n.1766+225A=
ENST00000527992.5:n.1212+225A=
ENST00000529510.5:n.672+225A=
ENST00000530407.5:n.1134+225A=
ENST00000532085.1:n.4590A=
ENST00000538950.5:c.765+225A=	ENSP00000475991.2:n.765+225A=
ENST00000545985.5:c.984+225A=	ENSP00000475241.2:n.984+225A=
NM_001164277.1:c.984+225A= , LRG_187t1:c.984+225A=	NP_001157749.1:n.984+225A=
NM_001164278.1:c.1000A=	NP_001157750.1:p.Thr334=
NM_001164279.1:c.765+225A=	NP_001157751.1:n.765+225A=
NM_001164280.1:c.984+225A=	NP_001157752.1:n.984+225A=
NM_001467.5:c.984+225A=	NP_001458.1:n.984+225A=
NM_001164278.2:c.1000A=	NP_001157750.1:p.Thr334=
NM_001164279.2:c.765+225A=	NP_001157751.1:n.765+225A=
NM_001164280.2:c.984+225A=	NP_001157752.1:n.984+225A=
NM_001467.6:c.984+225A=	NP_001458.1:n.984+225A=
NM_001164277.2:c.984+225A= MANE Select	NP_001157749.1:n.984+225A=