Canonical Allele Identifier: CA2003775346

Gene: SLC37A4

Linked Data

• dbSNP Id: rs782361210

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029390A>G , CM000673.2:g.119029390A>G	GRCh38
NC_000011.9:g.118900100A>G , CM000673.1:g.118900100A>G	GRCh37
NC_000011.8:g.118405310A>G	NCBI36
NG_013331.1:g.6517T>C , LRG_187:g.6517T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.209T>C
ENST00000697846.1:n.209T>C
ENST00000697847.1:n.209T>C
ENST00000697848.1:n.209T>C
ENST00000697849.1:n.453T>C
ENST00000697850.1:n.209T>C
ENST00000697851.1:n.453T>C
ENST00000638186.1:n.283T>C
ENST00000638360.1:n.217T>C
ENST00000638925.1:n.216T>C
ENST00000650539.1:n.385T>C
ENST00000330775.9:c.-21T>C	ENSP00000476242.2:n.-21T>C
ENST00000357590.9:c.-21T>C	ENSP00000476176.2:n.-21T>C
ENST00000525039.5:n.403T>C
ENST00000525102.5:n.737T>C
ENST00000525787.1:n.275T>C
ENST00000526626.6:n.175T>C
ENST00000527992.5:n.207T>C
ENST00000530407.5:n.197+2T>C
ENST00000532085.1:n.1474T>C
ENST00000532888.6:n.175T>C
ENST00000534384.1:n.200T>C
ENST00000538950.5:c.-172+2T>C	ENSP00000475991.2:n.-172+2T>C
ENST00000545985.5:c.-21T>C	ENSP00000475241.2:n.-21T>C
NM_001164277.1:c.-21T>C , LRG_187t1:c.-21T>C	NP_001157749.1:n.-21T>C
NM_001164278.1:c.-21T>C	NP_001157750.1:n.-21T>C
NM_001164279.1:c.-172+2T>C	NP_001157751.1:n.-172+2T>C
NM_001164280.1:c.-21T>C	NP_001157752.1:n.-21T>C
NM_001467.5:c.-21T>C	NP_001458.1:n.-21T>C
NM_001164278.2:c.-21T>C	NP_001157750.1:n.-21T>C
NM_001164279.2:c.-172+2T>C	NP_001157751.1:n.-172+2T>C
NM_001164280.2:c.-21T>C	NP_001157752.1:n.-21T>C
NM_001467.6:c.-21T>C	NP_001458.1:n.-21T>C
NM_001164277.2:c.-21T>C MANE Select	NP_001157749.1:n.-21T>C