Canonical Allele Identifier: CA2585300236

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41363873_41363874del , CM000681.2:g.41363873_41363874del GRCh38
NC_000019.9:g.41869778_41869779del , CM000681.1:g.41869778_41869779del GRCh37
NC_000019.8:g.46561618_46561619del NCBI36
NG_013091.1:g.5303_5304del

Transcript Alleles

HGVS Amino-acid Change
ENST00000243578.8:c.-5+87_-5+88del (B9D2) MANE Select ENSP00000243578.2:n.-5+87_-5+88del
ENST00000675972.1:c.-112_-111del (B9D2) ENSP00000501911.1:n.-112_-111del
ENST00000243578.7:c.-5+87_-5+88del (B9D2) ENSP00000243578.2:n.-5+87_-5+88del
ENST00000539627.5:c.-30+12671_-30+12672del (TMEM91) ENSP00000441900.1:n.-30+12671_-30+12672del
ENST00000594416.1:c.-5+87_-5+88del (B9D2) ENSP00000469666.1:n.-5+87_-5+88del
ENST00000601597.1:n.135+87_135+88del (B9D2)
ENST00000604123.5:c.142+9558_142+9559del (TMEM91) ENSP00000474871.1:n.142+9558_142+9559del
ENST00000604424.1:n.350+12671_350+12672del
NM_030578.3:c.-5+87_-5+88del (B9D2) NP_085055.2:n.-5+87_-5+88del
XM_006723405.1:c.-5+87_-5+88del (B9D2) XP_006723468.1:n.-5+87_-5+88del
XM_011527349.1:c.-112_-111del (B9D2) XP_011525651.1:n.-112_-111del
XM_011527350.1:c.-72+87_-72+88del (B9D2) XP_011525652.1:n.-72+87_-72+88del
XM_011527349.2:c.-112_-111del (B9D2) XP_011525651.1:n.-112_-111del
XM_011527350.2:c.-72+87_-72+88del (B9D2) XP_011525652.1:n.-72+87_-72+88del
NM_030578.4:c.-5+87_-5+88del (B9D2) MANE Select NP_085055.2:n.-5+87_-5+88del