Canonical Allele Identifier: CA2336431406

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41364039G= , CM000681.2:g.41364039G= GRCh38
NC_000019.9:g.41869944G= , CM000681.1:g.41869944G= GRCh37
NC_000019.8:g.46561784G= NCBI36
NG_013091.1:g.5135C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000243578.8:c.-86C= (B9D2) MANE Select ENSP00000243578.2:n.-86C=
ENST00000243578.7:c.-86C= (B9D2) ENSP00000243578.2:n.-86C=
ENST00000539627.5:c.-30+12837G= (TMEM91) ENSP00000441900.1:n.-30+12837G=
ENST00000594416.1:c.-86C= (B9D2) ENSP00000469666.1:n.-86C=
ENST00000601597.1:n.54C= (B9D2)
ENST00000604123.5:c.142+9724G= (TMEM91) ENSP00000474871.1:n.142+9724G=
ENST00000604424.1:n.350+12837G=
NM_001098825.1:c.-86G= (TMEM91) NP_001092295.1:n.-86G=
NM_030578.3:c.-86C= (B9D2) NP_085055.2:n.-86C=
XM_006723405.1:c.-86C= (B9D2) XP_006723468.1:n.-86C=
XM_011527350.1:c.-153C= (B9D2) XP_011525652.1:n.-153C=
XM_011527350.2:c.-153C= (B9D2) XP_011525652.1:n.-153C=
NM_030578.4:c.-86C= (B9D2) MANE Select NP_085055.2:n.-86C=
NM_001369864.1:c.-343G= (TMEM91) NP_001356793.1:n.-343G=
NM_001098825.2:c.-86G= (TMEM91) NP_001092295.1:n.-86G=