Canonical Allele Identifier: CA13499539
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1243537
ClinVar RCV Id: RCV001645698
dbSNP Id: rs77180649

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119026552C>T , CM000673.2:g.119026552C>T GRCh38
NC_000011.9:g.118897262C>T , CM000673.1:g.118897262C>T GRCh37
NC_000011.8:g.118402472C>T NCBI36
NG_013331.1:g.9354G>A , LRG_187:g.9354G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000529510.6:n.1014+385G>A
ENST00000697845.1:n.1323G>A
ENST00000697846.1:n.1014+385G>A
ENST00000697847.1:n.1151G>A
ENST00000697848.1:n.1100+51G>A
ENST00000697849.1:n.2438G>A
ENST00000697850.1:n.1100+51G>A
ENST00000697851.1:n.2708+51G>A
ENST00000638186.1:n.1174+51G>A
ENST00000638360.1:n.1006+51G>A
ENST00000638925.1:n.1139+19G>A
ENST00000650539.1:n.1276+51G>A
ENST00000330775.9:c.870+51G>A ENSP00000476242.2:n.870+51G>A
ENST00000357590.9:c.870+51G>A ENSP00000476176.2:n.870+51G>A
ENST00000524428.5:n.1106+385G>A
ENST00000525039.5:n.1294+51G>A
ENST00000525102.5:n.1628+51G>A
ENST00000525372.5:n.922G>A
ENST00000526275.5:n.1652+51G>A
ENST00000527992.5:n.1098+51G>A
ENST00000529510.5:n.558+385G>A
ENST00000530407.5:n.1020+51G>A
ENST00000532085.1:n.3780G>A
ENST00000538950.5:c.651+51G>A ENSP00000475991.2:n.651+51G>A
ENST00000545985.5:c.870+51G>A ENSP00000475241.2:n.870+51G>A
NM_001164277.1:c.870+51G>A , LRG_187t1:c.870+51G>A NP_001157749.1:n.870+51G>A
NM_001164278.1:c.870+51G>A NP_001157750.1:n.870+51G>A
NM_001164279.1:c.651+51G>A NP_001157751.1:n.651+51G>A
NM_001164280.1:c.870+51G>A NP_001157752.1:n.870+51G>A
NM_001467.5:c.870+51G>A NP_001458.1:n.870+51G>A
NM_001164278.2:c.870+51G>A NP_001157750.1:n.870+51G>A
NM_001164279.2:c.651+51G>A NP_001157751.1:n.651+51G>A
NM_001164280.2:c.870+51G>A NP_001157752.1:n.870+51G>A
NM_001467.6:c.870+51G>A NP_001458.1:n.870+51G>A
NM_001164277.2:c.870+51G>A MANE Select NP_001157749.1:n.870+51G>A