Canonical Allele Identifier: CA2793831500
Gene: SLC37A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119027016_119027017insCA , CM000673.2:g.119027016_119027017insCA GRCh38
NC_000011.9:g.118897726_118897727insCA , CM000673.1:g.118897726_118897727insCA GRCh37
NC_000011.8:g.118402936_118402937insCA NCBI36
NG_013331.1:g.8889_8890insTG , LRG_187:g.8889_8890insTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.934_935insTG
ENST00000697845.1:n.858_859insTG
ENST00000697846.1:n.934_935insTG
ENST00000697847.1:n.934_935insTG
ENST00000697848.1:n.934_935insTG
ENST00000697849.1:n.1973_1974insTG
ENST00000697850.1:n.934_935insTG
ENST00000697851.1:n.2294_2295insTG
ENST00000638186.1:n.1008_1009insTG
ENST00000638360.1:n.840_841insTG
ENST00000638925.1:n.941_942insTG
ENST00000650539.1:n.1110_1111insTG
ENST00000330775.9:c.704_705insTG ENSP00000476242.2:p.Val236GlyfsTer5
ENST00000357590.9:c.704_705insTG ENSP00000476176.2:p.Val236GlyfsTer5
ENST00000524428.5:n.1026_1027insTG
ENST00000525039.5:n.1128_1129insTG
ENST00000525102.5:n.1462_1463insTG
ENST00000525372.5:n.705_706insTG
ENST00000526275.5:n.1486_1487insTG
ENST00000526626.6:n.667_668insTG
ENST00000527992.5:n.932_933insTG
ENST00000529510.5:n.478_479insTG
ENST00000530407.5:n.854_855insTG
ENST00000532085.1:n.3315_3316insTG
ENST00000532888.6:n.1000_1001insTG
ENST00000538950.5:c.485_486insTG ENSP00000475991.2:p.Val163GlyfsTer5
ENST00000545985.5:c.704_705insTG ENSP00000475241.2:p.Val236GlyfsTer5
NM_001164277.1:c.704_705insTG , LRG_187t1:c.704_705insTG NP_001157749.1:p.Val236GlyfsTer5
NM_001164278.1:c.704_705insTG NP_001157750.1:p.Val236GlyfsTer5
NM_001164279.1:c.485_486insTG NP_001157751.1:p.Val163GlyfsTer5
NM_001164280.1:c.704_705insTG NP_001157752.1:p.Val236GlyfsTer5
NM_001467.5:c.704_705insTG NP_001458.1:p.Val236GlyfsTer5
NM_001164278.2:c.704_705insTG NP_001157750.1:p.Val236GlyfsTer5
NM_001164279.2:c.485_486insTG NP_001157751.1:p.Val163GlyfsTer5
NM_001164280.2:c.704_705insTG NP_001157752.1:p.Val236GlyfsTer5
NM_001467.6:c.704_705insTG NP_001458.1:p.Val236GlyfsTer5
NM_001164277.2:c.704_705insTG MANE Select NP_001157749.1:p.Val236GlyfsTer5