Canonical Allele Identifier: CA2244625865

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4933925_4933953delinsTCAGAGCCCGCCCCCAGCCCGACCACCCC , CM000679.2:g.4933925_4933953delinsTCAGAGCCCGCCCCCAGCCCGACCACCCC GRCh38
NC_000017.10:g.4837220_4837248delinsTCAGAGCCCGCCCCCAGCCCGACCACCCC , CM000679.1:g.4837220_4837248delinsTCAGAGCCCGCCCCCAGCCCGACCACCCC GRCh37
NC_000017.9:g.4777961_4777989delinsTCAGAGCCCGCCCCCAGCCCGACCACCCC NCBI36
NG_008767.2:g.6631_6659delinsTCAGAGCCCGCCCCCAGCCCGACCACCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000329125.6:c.1321_1349delinsTCAGAGCCCGCCCCCAGCCCGACCACCCC (GP1BA) MANE Select ENSP00000329380.5:p.Ser441=
ENST00000649830.1:c.-888+389_-888+417delinsGGGGTGGTCGGGCTGGGGGCGGGCTCTGA (CHRNE) ENSP00000496907.1:n.-888+389_-888+417delinsGGGGTGGTCGGGCTGGGG...
ENST00000329125.5:c.1321_1349delinsTCAGAGCCCGCCCCCAGCCCGACCACCCC (GP1BA) ENSP00000329380.5:p.Ser441=
ENST00000611961.1:c.1273-30_1273-2delinsTCAGAGCCCGCCCCCAGCCCGACCACCCC (GP1BA) ENSP00000484439.1:n.1273-30_1273-2delinsTCAGAGCCCGCCCCCAGCCCG...
NM_000173.6:c.1321_1349delinsTCAGAGCCCGCCCCCAGCCCGACCACCCC (GP1BA) NP_000164.5:p.Ser441=
NM_000173.7:c.1321_1349delinsTCAGAGCCCGCCCCCAGCCCGACCACCCC (GP1BA) MANE Select NP_000164.5:p.Ser441=