Canonical Allele Identifier: CA2616340716
Gene: SLC37A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119029463G>C , CM000673.2:g.119029463G>C GRCh38
NC_000011.9:g.118900173G>C , CM000673.1:g.118900173G>C GRCh37
NC_000011.8:g.118405383G>C NCBI36
NG_013331.1:g.6444C>G , LRG_187:g.6444C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.136C>G
ENST00000697846.1:n.136C>G
ENST00000697847.1:n.136C>G
ENST00000697848.1:n.136C>G
ENST00000697849.1:n.380C>G
ENST00000697850.1:n.136C>G
ENST00000697851.1:n.380C>G
ENST00000638186.1:n.210C>G
ENST00000638360.1:n.144C>G
ENST00000638925.1:n.143C>G
ENST00000650539.1:n.312C>G
ENST00000330775.9:c.-94C>G ENSP00000476242.2:n.-94C>G
ENST00000357590.9:c.-94C>G ENSP00000476176.2:n.-94C>G
ENST00000525039.5:n.330C>G
ENST00000525102.5:n.664C>G
ENST00000525787.1:n.202C>G
ENST00000526626.6:n.102C>G
ENST00000527992.5:n.134C>G
ENST00000530407.5:n.126C>G
ENST00000532085.1:n.1401C>G
ENST00000532888.6:n.102C>G
ENST00000534384.1:n.127C>G
ENST00000538950.5:c.-243C>G ENSP00000475991.2:n.-243C>G
ENST00000545985.5:c.-94C>G ENSP00000475241.2:n.-94C>G
NM_001164277.1:c.-94C>G , LRG_187t1:c.-94C>G NP_001157749.1:n.-94C>G
NM_001164278.1:c.-94C>G NP_001157750.1:n.-94C>G
NM_001164279.1:c.-243C>G NP_001157751.1:n.-243C>G
NM_001164280.1:c.-94C>G NP_001157752.1:n.-94C>G
NM_001467.5:c.-94C>G NP_001458.1:n.-94C>G
NM_001164278.2:c.-94C>G NP_001157750.1:n.-94C>G
NM_001164279.2:c.-243C>G NP_001157751.1:n.-243C>G
NM_001164280.2:c.-94C>G NP_001157752.1:n.-94C>G
NM_001467.6:c.-94C>G NP_001458.1:n.-94C>G
NM_001164277.2:c.-94C>G MANE Select NP_001157749.1:n.-94C>G