Canonical Allele Identifier: CA6311942
Gene: SLC37A4 HGNC NCBI

Linked Data

dbSNP Id: rs782311707

Genomic Alleles

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

Transcript Alleles

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