Canonical Allele Identifier: CA2003749640

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027630T= , CM000673.2:g.119027630T=	GRCh38
NC_000011.9:g.118898340T= , CM000673.1:g.118898340T=	GRCh37
NC_000011.8:g.118403550T=	NCBI36
NG_013331.1:g.8276A= , LRG_187:g.8276A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.853A=
ENST00000697845.1:n.777A=
ENST00000697846.1:n.853A=
ENST00000697847.1:n.853A=
ENST00000697848.1:n.853A=
ENST00000697849.1:n.1892A=
ENST00000697850.1:n.853A=
ENST00000697851.1:n.2213A=
ENST00000638186.1:n.927A=
ENST00000638360.1:n.759A=
ENST00000638925.1:n.860A=
ENST00000650539.1:n.1029A=
ENST00000330775.9:c.623A=	ENSP00000476242.2:p.Lys208=
ENST00000357590.9:c.623A=	ENSP00000476176.2:p.Lys208=
ENST00000524428.5:n.945A=
ENST00000525039.5:n.1047A=
ENST00000525102.5:n.1381A=
ENST00000525372.5:n.624A=
ENST00000526275.5:n.1405A=
ENST00000526626.6:n.586A=
ENST00000527992.5:n.851A=
ENST00000529510.5:n.400-535A=
ENST00000530407.5:n.773A=
ENST00000532085.1:n.3234A=
ENST00000532888.6:n.919A=
ENST00000538950.5:c.404A=	ENSP00000475991.2:p.Lys135=
ENST00000545985.5:c.623A=	ENSP00000475241.2:p.Lys208=
NM_001164277.1:c.623A= , LRG_187t1:c.623A=	NP_001157749.1:p.Lys208=
NM_001164278.1:c.623A=	NP_001157750.1:p.Lys208=
NM_001164279.1:c.404A=	NP_001157751.1:p.Lys135=
NM_001164280.1:c.623A=	NP_001157752.1:p.Lys208=
NM_001467.5:c.623A=	NP_001458.1:p.Lys208=
NM_001164278.2:c.623A=	NP_001157750.1:p.Lys208=
NM_001164279.2:c.404A=	NP_001157751.1:p.Lys135=
NM_001164280.2:c.623A=	NP_001157752.1:p.Lys208=
NM_001467.6:c.623A=	NP_001458.1:p.Lys208=
NM_001164277.2:c.623A= MANE Select	NP_001157749.1:p.Lys208=