Canonical Allele Identifier: CA2003748878
Gene: SLC37A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119026084T= , CM000673.2:g.119026084T= GRCh38
NC_000011.9:g.118896794T= , CM000673.1:g.118896794T= GRCh37
NC_000011.8:g.118402004T= NCBI36
NG_013331.1:g.9822A= , LRG_187:g.9822A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.1015-4A=
ENST00000697845.1:n.1791A=
ENST00000697846.1:n.1015-4A=
ENST00000697847.1:n.1202-327A=
ENST00000697848.1:n.1101-4A=
ENST00000697849.1:n.2906A=
ENST00000697850.1:n.1101-4A=
ENST00000697851.1:n.2709-4A=
ENST00000638186.1:n.1175-4A=
ENST00000638360.1:n.1007-4A=
ENST00000638925.1:n.1140-4A=
ENST00000650539.1:n.1277-4A=
ENST00000330775.9:c.871-4A= ENSP00000476242.2:n.871-4A=
ENST00000357590.9:c.871-4A= ENSP00000476176.2:n.871-4A=
ENST00000524428.5:n.1107-4A=
ENST00000525039.5:n.1295-4A=
ENST00000525102.5:n.1629-4A=
ENST00000525372.5:n.969-4A=
ENST00000526275.5:n.1653-4A=
ENST00000527992.5:n.1099-4A=
ENST00000529510.5:n.559-4A=
ENST00000530407.5:n.1021-4A=
ENST00000532085.1:n.4248A=
ENST00000538950.5:c.652-4A= ENSP00000475991.2:n.652-4A=
ENST00000545985.5:c.871-4A= ENSP00000475241.2:n.871-4A=
NM_001164277.1:c.871-4A= , LRG_187t1:c.871-4A= NP_001157749.1:n.871-4A=
NM_001164278.1:c.871-4A= NP_001157750.1:n.871-4A=
NM_001164279.1:c.652-4A= NP_001157751.1:n.652-4A=
NM_001164280.1:c.871-4A= NP_001157752.1:n.871-4A=
NM_001467.5:c.871-4A= NP_001458.1:n.871-4A=
NM_001164278.2:c.871-4A= NP_001157750.1:n.871-4A=
NM_001164279.2:c.652-4A= NP_001157751.1:n.652-4A=
NM_001164280.2:c.871-4A= NP_001157752.1:n.871-4A=
NM_001467.6:c.871-4A= NP_001458.1:n.871-4A=
NM_001164277.2:c.871-4A= MANE Select NP_001157749.1:n.871-4A=