Canonical Allele Identifier: CA2616340657
Gene: SLC37A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119029374G>A , CM000673.2:g.119029374G>A GRCh38
NC_000011.9:g.118900084G>A , CM000673.1:g.118900084G>A GRCh37
NC_000011.8:g.118405294G>A NCBI36
NG_013331.1:g.6533C>T , LRG_187:g.6533C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.225C>T
ENST00000697846.1:n.225C>T
ENST00000697847.1:n.225C>T
ENST00000697848.1:n.225C>T
ENST00000697849.1:n.469C>T
ENST00000697850.1:n.225C>T
ENST00000697851.1:n.469C>T
ENST00000638186.1:n.299C>T
ENST00000638360.1:n.233C>T
ENST00000638925.1:n.232C>T
ENST00000650539.1:n.401C>T
ENST00000330775.9:c.-5C>T ENSP00000476242.2:n.-5C>T
ENST00000357590.9:c.-5C>T ENSP00000476176.2:n.-5C>T
ENST00000525039.5:n.419C>T
ENST00000525102.5:n.753C>T
ENST00000525787.1:n.291C>T
ENST00000526626.6:n.191C>T
ENST00000527992.5:n.223C>T
ENST00000529510.5:n.14C>T
ENST00000530407.5:n.197+18C>T
ENST00000532085.1:n.1490C>T
ENST00000532888.6:n.191C>T
ENST00000534384.1:n.216C>T
ENST00000538950.5:c.-172+18C>T ENSP00000475991.2:n.-172+18C>T
ENST00000545985.5:c.-5C>T ENSP00000475241.2:n.-5C>T
NM_001164277.1:c.-5C>T , LRG_187t1:c.-5C>T NP_001157749.1:n.-5C>T
NM_001164278.1:c.-5C>T NP_001157750.1:n.-5C>T
NM_001164279.1:c.-172+18C>T NP_001157751.1:n.-172+18C>T
NM_001164280.1:c.-5C>T NP_001157752.1:n.-5C>T
NM_001467.5:c.-5C>T NP_001458.1:n.-5C>T
NM_001164278.2:c.-5C>T NP_001157750.1:n.-5C>T
NM_001164279.2:c.-172+18C>T NP_001157751.1:n.-172+18C>T
NM_001164280.2:c.-5C>T NP_001157752.1:n.-5C>T
NM_001467.6:c.-5C>T NP_001458.1:n.-5C>T
NM_001164277.2:c.-5C>T MANE Select NP_001157749.1:n.-5C>T