Canonical Allele Identifier: CA2003749752

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027821T= , CM000673.2:g.119027821T=	GRCh38
NC_000011.9:g.118898531T= , CM000673.1:g.118898531T=	GRCh37
NC_000011.8:g.118403741T=	NCBI36
NG_013331.1:g.8086A= , LRG_187:g.8086A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.662A=
ENST00000697845.1:n.586A=
ENST00000697846.1:n.662A=
ENST00000697847.1:n.662A=
ENST00000697848.1:n.662A=
ENST00000697849.1:n.1701A=
ENST00000697850.1:n.662A=
ENST00000697851.1:n.2022A=
ENST00000638186.1:n.736A=
ENST00000638360.1:n.619-51A=
ENST00000638925.1:n.669A=
ENST00000650539.1:n.838A=
ENST00000330775.9:c.433A=	ENSP00000476242.2:p.Met145=
ENST00000357590.9:c.433A=	ENSP00000476176.2:p.Met145=
ENST00000524428.5:n.754A=
ENST00000525039.5:n.856A=
ENST00000525102.5:n.1190A=
ENST00000525372.5:n.433A=
ENST00000525787.1:n.1049A=
ENST00000526275.5:n.1214A=
ENST00000526626.6:n.395A=
ENST00000527992.5:n.660A=
ENST00000529510.5:n.399+373A=
ENST00000530407.5:n.582A=
ENST00000532085.1:n.3043A=
ENST00000532888.6:n.728A=
ENST00000538950.5:c.214A=	ENSP00000475991.2:p.Met72=
ENST00000545985.5:c.433A=	ENSP00000475241.2:p.Met145=
NM_001164277.1:c.433A= , LRG_187t1:c.433A=	NP_001157749.1:p.Met145=
NM_001164278.1:c.433A=	NP_001157750.1:p.Met145=
NM_001164279.1:c.214A=	NP_001157751.1:p.Met72=
NM_001164280.1:c.433A=	NP_001157752.1:p.Met145=
NM_001467.5:c.433A=	NP_001458.1:p.Met145=
NM_001164278.2:c.433A=	NP_001157750.1:p.Met145=
NM_001164279.2:c.214A=	NP_001157751.1:p.Met72=
NM_001164280.2:c.433A=	NP_001157752.1:p.Met145=
NM_001467.6:c.433A=	NP_001458.1:p.Met145=
NM_001164277.2:c.433A= MANE Select	NP_001157749.1:p.Met145=