Canonical Allele Identifier: CA2003748780
Gene: SLC37A4 HGNC NCBI

Linked Data

dbSNP Id: rs1943551906

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119025927_119025928insA , CM000673.2:g.119025927_119025928insA GRCh38
NC_000011.9:g.118896637_118896638insA , CM000673.1:g.118896637_118896638insA GRCh37
NC_000011.8:g.118401847_118401848insA NCBI36
NG_013331.1:g.9978_9979insT , LRG_187:g.9978_9979insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.1128+39_1128+40insT
ENST00000697845.1:n.1947_1948insT
ENST00000697846.1:n.1128+39_1128+40insT
ENST00000697847.1:n.1202-171_1202-170insT
ENST00000697848.1:n.1214+39_1214+40insT
ENST00000697849.1:n.3062_3063insT
ENST00000697850.1:n.1253_1254insT
ENST00000697851.1:n.2822+39_2822+40insT
ENST00000638186.1:n.1288+39_1288+40insT
ENST00000638360.1:n.1120+39_1120+40insT
ENST00000638925.1:n.1253+39_1253+40insT
ENST00000650539.1:n.1390+39_1390+40insT
ENST00000330775.9:c.984+39_984+40insT ENSP00000476242.2:n.984+39_984+40insT
ENST00000357590.9:c.984+39_984+40insT ENSP00000476176.2:n.984+39_984+40insT
ENST00000524428.5:n.1220+39_1220+40insT
ENST00000525039.5:n.1408+39_1408+40insT
ENST00000525102.5:n.1742+39_1742+40insT
ENST00000525372.5:n.1082+39_1082+40insT
ENST00000526275.5:n.1766+39_1766+40insT
ENST00000527992.5:n.1212+39_1212+40insT
ENST00000529510.5:n.672+39_672+40insT
ENST00000530407.5:n.1134+39_1134+40insT
ENST00000532085.1:n.4404_4405insT
ENST00000538950.5:c.765+39_765+40insT ENSP00000475991.2:n.765+39_765+40insT
ENST00000545985.5:c.984+39_984+40insT ENSP00000475241.2:n.984+39_984+40insT
NM_001164277.1:c.984+39_984+40insT , LRG_187t1:c.984+39_984+40insT NP_001157749.1:n.984+39_984+40insT
NM_001164278.1:c.984+39_984+40insT NP_001157750.1:n.984+39_984+40insT
NM_001164279.1:c.765+39_765+40insT NP_001157751.1:n.765+39_765+40insT
NM_001164280.1:c.984+39_984+40insT NP_001157752.1:n.984+39_984+40insT
NM_001467.5:c.984+39_984+40insT NP_001458.1:n.984+39_984+40insT
NM_001164278.2:c.984+39_984+40insT NP_001157750.1:n.984+39_984+40insT
NM_001164279.2:c.765+39_765+40insT NP_001157751.1:n.765+39_765+40insT
NM_001164280.2:c.984+39_984+40insT NP_001157752.1:n.984+39_984+40insT
NM_001467.6:c.984+39_984+40insT NP_001458.1:n.984+39_984+40insT
NM_001164277.2:c.984+39_984+40insT MANE Select NP_001157749.1:n.984+39_984+40insT