Canonical Allele Identifier: CA2003775400
Gene: SLC37A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119029412T= , CM000673.2:g.119029412T= GRCh38
NC_000011.9:g.118900122T= , CM000673.1:g.118900122T= GRCh37
NC_000011.8:g.118405332T= NCBI36
NG_013331.1:g.6495A= , LRG_187:g.6495A=

Transcript Alleles

HGVS Amino-acid change
ENST00000529510.6:n.187A=
ENST00000697846.1:n.187A=
ENST00000697847.1:n.187A=
ENST00000697848.1:n.187A=
ENST00000697849.1:n.431A=
ENST00000697850.1:n.187A=
ENST00000697851.1:n.431A=
ENST00000638186.1:n.261A=
ENST00000638360.1:n.195A=
ENST00000638925.1:n.194A=
ENST00000650539.1:n.363A=
ENST00000330775.9:c.-43A= ENSP00000476242.2:n.-43A=
ENST00000357590.9:c.-43A= ENSP00000476176.2:n.-43A=
ENST00000525039.5:n.381A=
ENST00000525102.5:n.715A=
ENST00000525787.1:n.253A=
ENST00000526626.6:n.153A=
ENST00000527992.5:n.185A=
ENST00000530407.5:n.177A=
ENST00000532085.1:n.1452A=
ENST00000532888.6:n.153A=
ENST00000534384.1:n.178A=
ENST00000538950.5:c.-192A= ENSP00000475991.2:n.-192A=
ENST00000545985.5:c.-43A= ENSP00000475241.2:n.-43A=
NM_001164277.1:c.-43A= , LRG_187t1:c.-43A= NP_001157749.1:n.-43A=
NM_001164278.1:c.-43A= NP_001157750.1:n.-43A=
NM_001164279.1:c.-192A= NP_001157751.1:n.-192A=
NM_001164280.1:c.-43A= NP_001157752.1:n.-43A=
NM_001467.5:c.-43A= NP_001458.1:n.-43A=
NM_001164278.2:c.-43A= NP_001157750.1:n.-43A=
NM_001164279.2:c.-192A= NP_001157751.1:n.-192A=
NM_001164280.2:c.-43A= NP_001157752.1:n.-43A=
NM_001467.6:c.-43A= NP_001458.1:n.-43A=
NM_001164277.2:c.-43A= MANE Select NP_001157749.1:n.-43A=