Canonical Allele Identifier: CA2003775321
Gene: SLC37A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119029384G= , CM000673.2:g.119029384G= GRCh38
NC_000011.9:g.118900094G= , CM000673.1:g.118900094G= GRCh37
NC_000011.8:g.118405304G= NCBI36
NG_013331.1:g.6523C= , LRG_187:g.6523C=

Transcript Alleles

HGVS Amino-acid change
ENST00000529510.6:n.215C=
ENST00000697846.1:n.215C=
ENST00000697847.1:n.215C=
ENST00000697848.1:n.215C=
ENST00000697849.1:n.459C=
ENST00000697850.1:n.215C=
ENST00000697851.1:n.459C=
ENST00000638186.1:n.289C=
ENST00000638360.1:n.223C=
ENST00000638925.1:n.222C=
ENST00000650539.1:n.391C=
ENST00000330775.9:c.-15C= ENSP00000476242.2:n.-15C=
ENST00000357590.9:c.-15C= ENSP00000476176.2:n.-15C=
ENST00000525039.5:n.409C=
ENST00000525102.5:n.743C=
ENST00000525787.1:n.281C=
ENST00000526626.6:n.181C=
ENST00000527992.5:n.213C=
ENST00000529510.5:n.4C=
ENST00000530407.5:n.197+8C=
ENST00000532085.1:n.1480C=
ENST00000532888.6:n.181C=
ENST00000534384.1:n.206C=
ENST00000538950.5:c.-172+8C= ENSP00000475991.2:n.-172+8C=
ENST00000545985.5:c.-15C= ENSP00000475241.2:n.-15C=
NM_001164277.1:c.-15C= , LRG_187t1:c.-15C= NP_001157749.1:n.-15C=
NM_001164278.1:c.-15C= NP_001157750.1:n.-15C=
NM_001164279.1:c.-172+8C= NP_001157751.1:n.-172+8C=
NM_001164280.1:c.-15C= NP_001157752.1:n.-15C=
NM_001467.5:c.-15C= NP_001458.1:n.-15C=
NM_001164278.2:c.-15C= NP_001157750.1:n.-15C=
NM_001164279.2:c.-172+8C= NP_001157751.1:n.-172+8C=
NM_001164280.2:c.-15C= NP_001157752.1:n.-15C=
NM_001467.6:c.-15C= NP_001458.1:n.-15C=
NM_001164277.2:c.-15C= MANE Select NP_001157749.1:n.-15C=