Canonical Allele Identifier: CA2003775334
Gene: SLC37A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119029386C= , CM000673.2:g.119029386C= GRCh38
NC_000011.9:g.118900096C= , CM000673.1:g.118900096C= GRCh37
NC_000011.8:g.118405306C= NCBI36
NG_013331.1:g.6521G= , LRG_187:g.6521G=

Transcript Alleles

HGVS Amino-acid change
ENST00000529510.6:n.213G=
ENST00000697846.1:n.213G=
ENST00000697847.1:n.213G=
ENST00000697848.1:n.213G=
ENST00000697849.1:n.457G=
ENST00000697850.1:n.213G=
ENST00000697851.1:n.457G=
ENST00000638186.1:n.287G=
ENST00000638360.1:n.221G=
ENST00000638925.1:n.220G=
ENST00000650539.1:n.389G=
ENST00000330775.9:c.-17G= ENSP00000476242.2:n.-17G=
ENST00000357590.9:c.-17G= ENSP00000476176.2:n.-17G=
ENST00000525039.5:n.407G=
ENST00000525102.5:n.741G=
ENST00000525787.1:n.279G=
ENST00000526626.6:n.179G=
ENST00000527992.5:n.211G=
ENST00000529510.5:n.2G=
ENST00000530407.5:n.197+6G=
ENST00000532085.1:n.1478G=
ENST00000532888.6:n.179G=
ENST00000534384.1:n.204G=
ENST00000538950.5:c.-172+6G= ENSP00000475991.2:n.-172+6G=
ENST00000545985.5:c.-17G= ENSP00000475241.2:n.-17G=
NM_001164277.1:c.-17G= , LRG_187t1:c.-17G= NP_001157749.1:n.-17G=
NM_001164278.1:c.-17G= NP_001157750.1:n.-17G=
NM_001164279.1:c.-172+6G= NP_001157751.1:n.-172+6G=
NM_001164280.1:c.-17G= NP_001157752.1:n.-17G=
NM_001467.5:c.-17G= NP_001458.1:n.-17G=
NM_001164278.2:c.-17G= NP_001157750.1:n.-17G=
NM_001164279.2:c.-172+6G= NP_001157751.1:n.-172+6G=
NM_001164280.2:c.-17G= NP_001157752.1:n.-17G=
NM_001467.6:c.-17G= NP_001458.1:n.-17G=
NM_001164277.2:c.-17G= MANE Select NP_001157749.1:n.-17G=