Canonical Allele Identifier: CA2635579204

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4933901_4933910del , CM000679.2:g.4933901_4933910del GRCh38
NC_000017.10:g.4837196_4837205del , CM000679.1:g.4837196_4837205del GRCh37
NG_008767.2:g.6607_6616del

Transcript Alleles

HGVS Amino-acid Change
ENST00000329125.6:c.1297_1306del (GP1BA) MANE Select ENSP00000329380.5:p.Ser433ProfsTer?
ENST00000649830.1:c.-888+432_-888+441del (CHRNE) ENSP00000496907.1:n.-888+432_-888+441del
ENST00000329125.5:c.1297_1306del (GP1BA) ENSP00000329380.5:p.Ser433ProfsTer?
ENST00000611961.1:c.1272+25_1272+34del (GP1BA) ENSP00000484439.1:n.1272+25_1272+34del
NM_000173.6:c.1297_1306del (GP1BA) NP_000164.5:p.Ser433ProfsTer?
NM_000173.7:c.1297_1306del (GP1BA) MANE Select NP_000164.5:p.Ser433ProfsTer?