Canonical Allele Identifier: CA912970984
Gene: SLC37A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119026624_119026628del , CM000673.2:g.119026624_119026628del GRCh38
NC_000011.9:g.118897334_118897338del , CM000673.1:g.118897334_118897338del GRCh37
NC_000011.8:g.118402544_118402548del NCBI36
NG_013331.1:g.9278_9282del , LRG_187:g.9278_9282del

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.1014+309_1014+313del
ENST00000697845.1:n.1247_1251del
ENST00000697846.1:n.1014+309_1014+313del
ENST00000697847.1:n.1075_1079del
ENST00000697848.1:n.1075_1079del
ENST00000697849.1:n.2362_2366del
ENST00000697850.1:n.1075_1079del
ENST00000697851.1:n.2683_2687del
ENST00000638186.1:n.1149_1153del
ENST00000638360.1:n.981_985del
ENST00000638925.1:n.1082_1086del
ENST00000650539.1:n.1251_1255del
ENST00000330775.9:c.845_849del ENSP00000476242.2:p.Tyr282PhefsTer?
ENST00000357590.9:c.845_849del ENSP00000476176.2:p.Tyr282PhefsTer?
ENST00000524428.5:n.1106+309_1106+313del
ENST00000525039.5:n.1269_1273del
ENST00000525102.5:n.1603_1607del
ENST00000525372.5:n.846_850del
ENST00000526275.5:n.1627_1631del
ENST00000527992.5:n.1073_1077del
ENST00000529510.5:n.558+309_558+313del
ENST00000530407.5:n.995_999del
ENST00000532085.1:n.3704_3708del
ENST00000538950.5:c.626_630del ENSP00000475991.2:p.Tyr209PhefsTer?
ENST00000545985.5:c.845_849del ENSP00000475241.2:p.Tyr282PhefsTer?
NM_001164277.1:c.845_849del , LRG_187t1:c.845_849del NP_001157749.1:p.Tyr282PhefsTer?
NM_001164278.1:c.845_849del NP_001157750.1:p.Tyr282PhefsTer?
NM_001164279.1:c.626_630del NP_001157751.1:p.Tyr209PhefsTer?
NM_001164280.1:c.845_849del NP_001157752.1:p.Tyr282PhefsTer?
NM_001467.5:c.845_849del NP_001458.1:p.Tyr282PhefsTer?
NM_001164278.2:c.845_849del NP_001157750.1:p.Tyr282PhefsTer?
NM_001164279.2:c.626_630del NP_001157751.1:p.Tyr209PhefsTer?
NM_001164280.2:c.845_849del NP_001157752.1:p.Tyr282PhefsTer?
NM_001467.6:c.845_849del NP_001458.1:p.Tyr282PhefsTer?
NM_001164277.2:c.845_849del MANE Select NP_001157749.1:p.Tyr282PhefsTer?