Canonical Allele Identifier: CA382901127
Gene: SLC37A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119026988C>T , CM000673.2:g.119026988C>T GRCh38
NC_000011.9:g.118897698C>T , CM000673.1:g.118897698C>T GRCh37
NC_000011.8:g.118402908C>T NCBI36
NG_013331.1:g.8918G>A , LRG_187:g.8918G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000529510.6:n.963G>A
ENST00000697845.1:n.887G>A
ENST00000697846.1:n.963G>A
ENST00000697847.1:n.963G>A
ENST00000697848.1:n.963G>A
ENST00000697849.1:n.2002G>A
ENST00000697850.1:n.963G>A
ENST00000697851.1:n.2323G>A
ENST00000638186.1:n.1037G>A
ENST00000638360.1:n.869G>A
ENST00000638925.1:n.970G>A
ENST00000650539.1:n.1139G>A
ENST00000330775.9:c.733G>A ENSP00000476242.2:p.Asp245Asn
ENST00000357590.9:c.733G>A ENSP00000476176.2:p.Asp245Asn
ENST00000524428.5:n.1055G>A
ENST00000525039.5:n.1157G>A
ENST00000525102.5:n.1491G>A
ENST00000525372.5:n.734G>A
ENST00000526275.5:n.1515G>A
ENST00000526626.6:n.696G>A
ENST00000527992.5:n.961G>A
ENST00000529510.5:n.507G>A
ENST00000530407.5:n.883G>A
ENST00000532085.1:n.3344G>A
ENST00000532888.6:n.1029G>A
ENST00000538950.5:c.514G>A ENSP00000475991.2:p.Asp172Asn
ENST00000545985.5:c.733G>A ENSP00000475241.2:p.Asp245Asn
NM_001164277.1:c.733G>A , LRG_187t1:c.733G>A NP_001157749.1:p.Asp245Asn
NM_001164278.1:c.733G>A NP_001157750.1:p.Asp245Asn
NM_001164279.1:c.514G>A NP_001157751.1:p.Asp172Asn
NM_001164280.1:c.733G>A NP_001157752.1:p.Asp245Asn
NM_001467.5:c.733G>A NP_001458.1:p.Asp245Asn
NM_001164278.2:c.733G>A NP_001157750.1:p.Asp245Asn
NM_001164279.2:c.514G>A NP_001157751.1:p.Asp172Asn
NM_001164280.2:c.733G>A NP_001157752.1:p.Asp245Asn
NM_001467.6:c.733G>A NP_001458.1:p.Asp245Asn
NM_001164277.2:c.733G>A MANE Select NP_001157749.1:p.Asp245Asn