Canonical Allele Identifier: CA2244625863

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4933925_4933944delinsTCAGAGCCCGCCCCCAGCCC , CM000679.2:g.4933925_4933944delinsTCAGAGCCCGCCCCCAGCCC GRCh38
NC_000017.10:g.4837220_4837239delinsTCAGAGCCCGCCCCCAGCCC , CM000679.1:g.4837220_4837239delinsTCAGAGCCCGCCCCCAGCCC GRCh37
NC_000017.9:g.4777961_4777980delinsTCAGAGCCCGCCCCCAGCCC NCBI36
NG_008767.2:g.6631_6650delinsTCAGAGCCCGCCCCCAGCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000329125.6:c.1321_1340delinsTCAGAGCCCGCCCCCAGCCC (GP1BA) MANE Select ENSP00000329380.5:p.Ser441=
ENST00000649830.1:c.-888+398_-888+417delinsGGGCTGGGGGCGGGCTCTGA (CHRNE) ENSP00000496907.1:n.-888+398_-888+417delinsGGGCTGGGGGCGGGCTCT...
ENST00000329125.5:c.1321_1340delinsTCAGAGCCCGCCCCCAGCCC (GP1BA) ENSP00000329380.5:p.Ser441=
ENST00000611961.1:c.1273-30_1273-11delinsTCAGAGCCCGCCCCCAGCCC (GP1BA) ENSP00000484439.1:n.1273-30_1273-11delinsTCAGAGCCCGCCCCCAGCCC...
NM_000173.6:c.1321_1340delinsTCAGAGCCCGCCCCCAGCCC (GP1BA) NP_000164.5:p.Ser441=
NM_000173.7:c.1321_1340delinsTCAGAGCCCGCCCCCAGCCC (GP1BA) MANE Select NP_000164.5:p.Ser441=