Canonical Allele Identifier: CA2628214352

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.44711390del , CM000677.2:g.44711390del GRCh38
NC_000015.9:g.45003588del , CM000677.1:g.45003588del GRCh37
NC_000015.8:g.42790880del NCBI36
NG_012920.1:g.4904del
NG_012920.2:g.4914del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695792.1:n.33del (B2M)
XM_011521338.1:c.-624del (PATL2) XP_011519640.1:n.-624del
XM_011521339.1:c.-505del (PATL2) XP_011519641.1:n.-505del
XM_011521340.1:c.-446del (PATL2) XP_011519642.1:n.-446del
XM_011521343.1:c.-708del (PATL2) XP_011519645.1:n.-708del
XM_011521345.1:c.-679del (PATL2) XP_011519647.1:n.-679del
XM_011521338.3:c.-624del (PATL2) XP_011519640.1:n.-624del
XM_011521339.3:c.-505del (PATL2) XP_011519641.1:n.-505del
XM_011521340.3:c.-446del (PATL2) XP_011519642.1:n.-446del
XM_011521343.3:c.-708del (PATL2) XP_011519645.1:n.-708del
XM_011521345.3:c.-679del (PATL2) XP_011519647.1:n.-679del
NM_001387260.1:c.-134del (PATL2) NP_001374189.1:n.-134del