Canonical Allele Identifier: CA2585300343

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41363982_41363983del , CM000681.2:g.41363982_41363983del GRCh38
NC_000019.9:g.41869887_41869888del , CM000681.1:g.41869887_41869888del GRCh37
NC_000019.8:g.46561727_46561728del NCBI36
NG_013091.1:g.5194_5195del

Transcript Alleles

HGVS Amino-acid Change
ENST00000243578.8:c.-27_-26del (B9D2) MANE Select ENSP00000243578.2:n.-27_-26del
ENST00000243578.7:c.-27_-26del (B9D2) ENSP00000243578.2:n.-27_-26del
ENST00000539627.5:c.-30+12780_-30+12781del (TMEM91) ENSP00000441900.1:n.-30+12780_-30+12781del
ENST00000594416.1:c.-27_-26del (B9D2) ENSP00000469666.1:n.-27_-26del
ENST00000601597.1:n.113_114del (B9D2)
ENST00000604123.5:c.142+9667_142+9668del (TMEM91) ENSP00000474871.1:n.142+9667_142+9668del
ENST00000604424.1:n.350+12780_350+12781del
NM_001098825.1:c.-143_-142del (TMEM91) NP_001092295.1:n.-143_-142del
NM_030578.3:c.-27_-26del (B9D2) NP_085055.2:n.-27_-26del
XM_006723405.1:c.-27_-26del (B9D2) XP_006723468.1:n.-27_-26del
XM_011527350.1:c.-94_-93del (B9D2) XP_011525652.1:n.-94_-93del
XM_011527350.2:c.-94_-93del (B9D2) XP_011525652.1:n.-94_-93del
NM_030578.4:c.-27_-26del (B9D2) MANE Select NP_085055.2:n.-27_-26del
NM_001369864.1:c.-400_-399del (TMEM91) NP_001356793.1:n.-400_-399del
NM_001098825.2:c.-143_-142del (TMEM91) NP_001092295.1:n.-143_-142del