Canonical Allele Identifier: CA2003748740
Gene: SLC37A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119025854_119025856delinsCTG , CM000673.2:g.119025854_119025856delinsCTG GRCh38
NC_000011.9:g.118896564_118896566delinsCTG , CM000673.1:g.118896564_118896566delinsCTG GRCh37
NC_000011.8:g.118401774_118401776delinsCTG NCBI36
NG_013331.1:g.10050_10052delinsCAG , LRG_187:g.10050_10052delinsCAG

Transcript Alleles

HGVS Amino-acid change
ENST00000529510.6:n.1129-99_1129-97delinsCAG
ENST00000697845.1:n.2019_2021delinsCAG
ENST00000697846.1:n.1129-99_1129-97delinsCAG
ENST00000697847.1:n.1202-99_1202-97delinsCAG
ENST00000697848.1:n.1215-99_1215-97delinsCAG
ENST00000697849.1:n.3134_3136delinsCAG
ENST00000697850.1:n.1325_1327delinsCAG
ENST00000697851.1:n.2822+111_2822+113delinsCAG
ENST00000638186.1:n.1288+111_1288+113delinsCAG
ENST00000638360.1:n.1120+111_1120+113delinsCAG
ENST00000638925.1:n.1253+111_1253+113delinsCAG
ENST00000650539.1:n.1391-99_1391-97delinsCAG
ENST00000330775.9:c.984+111_984+113delinsCAG ENSP00000476242.2:n.984+111_984+113delinsCAG
ENST00000357590.9:c.985-99_985-97delinsCAG ENSP00000476176.2:n.985-99_985-97delinsCAG
ENST00000524428.5:n.1220+111_1220+113delinsCAG
ENST00000525039.5:n.1409-99_1409-97delinsCAG
ENST00000525102.5:n.1742+111_1742+113delinsCAG
ENST00000525372.5:n.1082+111_1082+113delinsCAG
ENST00000526275.5:n.1766+111_1766+113delinsCAG
ENST00000527992.5:n.1212+111_1212+113delinsCAG
ENST00000529510.5:n.672+111_672+113delinsCAG
ENST00000530407.5:n.1134+111_1134+113delinsCAG
ENST00000532085.1:n.4476_4478delinsCAG
ENST00000538950.5:c.765+111_765+113delinsCAG ENSP00000475991.2:n.765+111_765+113delinsCAG
ENST00000545985.5:c.984+111_984+113delinsCAG ENSP00000475241.2:n.984+111_984+113delinsCAG
NM_001164277.1:c.984+111_984+113delinsCAG , LRG_187t1:c.984+111_984+113delinsCAG NP_001157749.1:n.984+111_984+113delinsCAG
NM_001164278.1:c.985-99_985-97delinsCAG NP_001157750.1:n.985-99_985-97delinsCAG
NM_001164279.1:c.765+111_765+113delinsCAG NP_001157751.1:n.765+111_765+113delinsCAG
NM_001164280.1:c.984+111_984+113delinsCAG NP_001157752.1:n.984+111_984+113delinsCAG
NM_001467.5:c.984+111_984+113delinsCAG NP_001458.1:n.984+111_984+113delinsCAG
NM_001164278.2:c.985-99_985-97delinsCAG NP_001157750.1:n.985-99_985-97delinsCAG
NM_001164279.2:c.765+111_765+113delinsCAG NP_001157751.1:n.765+111_765+113delinsCAG
NM_001164280.2:c.984+111_984+113delinsCAG NP_001157752.1:n.984+111_984+113delinsCAG
NM_001467.6:c.984+111_984+113delinsCAG NP_001458.1:n.984+111_984+113delinsCAG
NM_001164277.2:c.984+111_984+113delinsCAG MANE Select NP_001157749.1:n.984+111_984+113delinsCAG