Canonical Allele Identifier: CA6311941
Gene: SLC37A4 HGNC NCBI

Linked Data

dbSNP Id: rs782311707

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119029401C>T , CM000673.2:g.119029401C>T GRCh38
NC_000011.9:g.118900111C>T , CM000673.1:g.118900111C>T GRCh37
NC_000011.8:g.118405321C>T NCBI36
NG_013331.1:g.6506G>A , LRG_187:g.6506G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000529510.6:n.198G>A
ENST00000697846.1:n.198G>A
ENST00000697847.1:n.198G>A
ENST00000697848.1:n.198G>A
ENST00000697849.1:n.442G>A
ENST00000697850.1:n.198G>A
ENST00000697851.1:n.442G>A
ENST00000638186.1:n.272G>A
ENST00000638360.1:n.206G>A
ENST00000638925.1:n.205G>A
ENST00000650539.1:n.374G>A
ENST00000330775.9:c.-32G>A ENSP00000476242.2:n.-32G>A
ENST00000357590.9:c.-32G>A ENSP00000476176.2:n.-32G>A
ENST00000525039.5:n.392G>A
ENST00000525102.5:n.726G>A
ENST00000525787.1:n.264G>A
ENST00000526626.6:n.164G>A
ENST00000527992.5:n.196G>A
ENST00000530407.5:n.188G>A
ENST00000532085.1:n.1463G>A
ENST00000532888.6:n.164G>A
ENST00000534384.1:n.189G>A
ENST00000538950.5:c.-181G>A ENSP00000475991.2:n.-181G>A
ENST00000545985.5:c.-32G>A ENSP00000475241.2:n.-32G>A
NM_001164277.1:c.-32G>A , LRG_187t1:c.-32G>A NP_001157749.1:n.-32G>A
NM_001164278.1:c.-32G>A NP_001157750.1:n.-32G>A
NM_001164279.1:c.-181G>A NP_001157751.1:n.-181G>A
NM_001164280.1:c.-32G>A NP_001157752.1:n.-32G>A
NM_001467.5:c.-32G>A NP_001458.1:n.-32G>A
NM_001164278.2:c.-32G>A NP_001157750.1:n.-32G>A
NM_001164279.2:c.-181G>A NP_001157751.1:n.-181G>A
NM_001164280.2:c.-32G>A NP_001157752.1:n.-32G>A
NM_001467.6:c.-32G>A NP_001458.1:n.-32G>A
NM_001164277.2:c.-32G>A MANE Select NP_001157749.1:n.-32G>A