Canonical Allele Identifier: CA2616339930
Gene: SLC37A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119025862C>A , CM000673.2:g.119025862C>A GRCh38
NC_000011.9:g.118896572C>A , CM000673.1:g.118896572C>A GRCh37
NC_000011.8:g.118401782C>A NCBI36
NG_013331.1:g.10044G>T , LRG_187:g.10044G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.1129-105G>T
ENST00000697845.1:n.2013G>T
ENST00000697846.1:n.1129-105G>T
ENST00000697847.1:n.1202-105G>T
ENST00000697848.1:n.1215-105G>T
ENST00000697849.1:n.3128G>T
ENST00000697850.1:n.1319G>T
ENST00000697851.1:n.2822+105G>T
ENST00000638186.1:n.1288+105G>T
ENST00000638360.1:n.1120+105G>T
ENST00000638925.1:n.1253+105G>T
ENST00000650539.1:n.1391-105G>T
ENST00000330775.9:c.984+105G>T ENSP00000476242.2:n.984+105G>T
ENST00000357590.9:c.985-105G>T ENSP00000476176.2:n.985-105G>T
ENST00000524428.5:n.1220+105G>T
ENST00000525039.5:n.1409-105G>T
ENST00000525102.5:n.1742+105G>T
ENST00000525372.5:n.1082+105G>T
ENST00000526275.5:n.1766+105G>T
ENST00000527992.5:n.1212+105G>T
ENST00000529510.5:n.672+105G>T
ENST00000530407.5:n.1134+105G>T
ENST00000532085.1:n.4470G>T
ENST00000538950.5:c.765+105G>T ENSP00000475991.2:n.765+105G>T
ENST00000545985.5:c.984+105G>T ENSP00000475241.2:n.984+105G>T
NM_001164277.1:c.984+105G>T , LRG_187t1:c.984+105G>T NP_001157749.1:n.984+105G>T
NM_001164278.1:c.985-105G>T NP_001157750.1:n.985-105G>T
NM_001164279.1:c.765+105G>T NP_001157751.1:n.765+105G>T
NM_001164280.1:c.984+105G>T NP_001157752.1:n.984+105G>T
NM_001467.5:c.984+105G>T NP_001458.1:n.984+105G>T
NM_001164278.2:c.985-105G>T NP_001157750.1:n.985-105G>T
NM_001164279.2:c.765+105G>T NP_001157751.1:n.765+105G>T
NM_001164280.2:c.984+105G>T NP_001157752.1:n.984+105G>T
NM_001467.6:c.984+105G>T NP_001458.1:n.984+105G>T
NM_001164277.2:c.984+105G>T MANE Select NP_001157749.1:n.984+105G>T