Canonical Allele Identifier: CA2616340724
Gene: SLC37A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119029475T>C , CM000673.2:g.119029475T>C GRCh38
NC_000011.9:g.118900185T>C , CM000673.1:g.118900185T>C GRCh37
NC_000011.8:g.118405395T>C NCBI36
NG_013331.1:g.6432A>G , LRG_187:g.6432A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.124A>G
ENST00000697846.1:n.124A>G
ENST00000697847.1:n.124A>G
ENST00000697848.1:n.124A>G
ENST00000697849.1:n.368A>G
ENST00000697850.1:n.124A>G
ENST00000697851.1:n.368A>G
ENST00000638186.1:n.198A>G
ENST00000638360.1:n.132A>G
ENST00000638925.1:n.131A>G
ENST00000650539.1:n.300A>G
ENST00000330775.9:c.-106A>G ENSP00000476242.2:n.-106A>G
ENST00000357590.9:c.-106A>G ENSP00000476176.2:n.-106A>G
ENST00000525039.5:n.318A>G
ENST00000525102.5:n.652A>G
ENST00000525787.1:n.190A>G
ENST00000526626.6:n.90A>G
ENST00000527992.5:n.122A>G
ENST00000530407.5:n.114A>G
ENST00000532085.1:n.1389A>G
ENST00000532888.6:n.90A>G
ENST00000534384.1:n.115A>G
ENST00000538950.5:c.-255A>G ENSP00000475991.2:n.-255A>G
ENST00000545985.5:c.-106A>G ENSP00000475241.2:n.-106A>G
NM_001164277.1:c.-106A>G , LRG_187t1:c.-106A>G NP_001157749.1:n.-106A>G
NM_001164278.1:c.-106A>G NP_001157750.1:n.-106A>G
NM_001164279.1:c.-255A>G NP_001157751.1:n.-255A>G
NM_001164280.1:c.-106A>G NP_001157752.1:n.-106A>G
NM_001467.5:c.-106A>G NP_001458.1:n.-106A>G
NM_001164278.2:c.-106A>G NP_001157750.1:n.-106A>G
NM_001164279.2:c.-255A>G NP_001157751.1:n.-255A>G
NM_001164280.2:c.-106A>G NP_001157752.1:n.-106A>G
NM_001467.6:c.-106A>G NP_001458.1:n.-106A>G
NM_001164277.2:c.-106A>G MANE Select NP_001157749.1:n.-106A>G