Canonical Allele Identifier: CA2576136030

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4934056del , CM000679.2:g.4934056del GRCh38
NC_000017.10:g.4837351del , CM000679.1:g.4837351del GRCh37
NC_000017.9:g.4778092del NCBI36
NG_008767.2:g.6762del

Transcript Alleles

HGVS Amino-acid Change
ENST00000329125.6:c.1452del (GP1BA) MANE Select ENSP00000329380.5:p.Val485TyrfsTer4
ENST00000649830.1:c.-888+288del (CHRNE) ENSP00000496907.1:n.-888+288del
ENST00000329125.5:c.1452del (GP1BA) ENSP00000329380.5:p.Val485TyrfsTer4
ENST00000611961.1:c.1374del (GP1BA) ENSP00000484439.1:p.Val459TyrfsTer4
NM_000173.6:c.1452del (GP1BA) NP_000164.5:p.Val485TyrfsTer4
NM_000173.7:c.1452del (GP1BA) MANE Select NP_000164.5:p.Val485TyrfsTer4