Canonical Allele Identifier: CA2616339994
Gene: SLC37A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119026086G>A , CM000673.2:g.119026086G>A GRCh38
NC_000011.9:g.118896796G>A , CM000673.1:g.118896796G>A GRCh37
NC_000011.8:g.118402006G>A NCBI36
NG_013331.1:g.9820C>T , LRG_187:g.9820C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.1015-6C>T
ENST00000697845.1:n.1789C>T
ENST00000697846.1:n.1015-6C>T
ENST00000697847.1:n.1202-329C>T
ENST00000697848.1:n.1101-6C>T
ENST00000697849.1:n.2904C>T
ENST00000697850.1:n.1101-6C>T
ENST00000697851.1:n.2709-6C>T
ENST00000638186.1:n.1175-6C>T
ENST00000638360.1:n.1007-6C>T
ENST00000638925.1:n.1140-6C>T
ENST00000650539.1:n.1277-6C>T
ENST00000330775.9:c.871-6C>T ENSP00000476242.2:n.871-6C>T
ENST00000357590.9:c.871-6C>T ENSP00000476176.2:n.871-6C>T
ENST00000524428.5:n.1107-6C>T
ENST00000525039.5:n.1295-6C>T
ENST00000525102.5:n.1629-6C>T
ENST00000525372.5:n.969-6C>T
ENST00000526275.5:n.1653-6C>T
ENST00000527992.5:n.1099-6C>T
ENST00000529510.5:n.559-6C>T
ENST00000530407.5:n.1021-6C>T
ENST00000532085.1:n.4246C>T
ENST00000538950.5:c.652-6C>T ENSP00000475991.2:n.652-6C>T
ENST00000545985.5:c.871-6C>T ENSP00000475241.2:n.871-6C>T
NM_001164277.1:c.871-6C>T , LRG_187t1:c.871-6C>T NP_001157749.1:n.871-6C>T
NM_001164278.1:c.871-6C>T NP_001157750.1:n.871-6C>T
NM_001164279.1:c.652-6C>T NP_001157751.1:n.652-6C>T
NM_001164280.1:c.871-6C>T NP_001157752.1:n.871-6C>T
NM_001467.5:c.871-6C>T NP_001458.1:n.871-6C>T
NM_001164278.2:c.871-6C>T NP_001157750.1:n.871-6C>T
NM_001164279.2:c.652-6C>T NP_001157751.1:n.652-6C>T
NM_001164280.2:c.871-6C>T NP_001157752.1:n.871-6C>T
NM_001467.6:c.871-6C>T NP_001458.1:n.871-6C>T
NM_001164277.2:c.871-6C>T MANE Select NP_001157749.1:n.871-6C>T