Canonical Allele Identifier: CA2336427591

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41355577_41355578delinsTC , CM000681.2:g.41355577_41355578delinsTC GRCh38
NC_000019.9:g.41861482_41861483delinsTC , CM000681.1:g.41861482_41861483delinsTC GRCh37
NC_000019.8:g.46553322_46553323delinsTC NCBI36
NG_013091.1:g.13596_13597delinsGA
NG_013364.1:g.3349_3350delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000243578.8:c.215-565_215-564delinsGA (B9D2) MANE Select ENSP00000243578.2:n.215-565_215-564delinsGA
ENST00000675972.1:c.215-565_215-564delinsGA (B9D2) ENSP00000501911.1:n.215-565_215-564delinsGA
ENST00000243578.7:c.215-565_215-564delinsGA (B9D2) ENSP00000243578.2:n.215-565_215-564delinsGA
ENST00000539627.5:c.-30+4375_-30+4376delinsTC (TMEM91) ENSP00000441900.1:n.-30+4375_-30+4376delinsTC
ENST00000594416.1:c.*61-565_*61-564delinsGA (B9D2) ENSP00000469666.1:n.*61-565_*61-564delinsGA
ENST00000604123.5:c.142+1262_142+1263delinsTC (TMEM91) ENSP00000474871.1:n.142+1262_142+1263delinsTC
ENST00000604424.1:n.350+4375_350+4376delinsTC
NM_030578.3:c.215-565_215-564delinsGA (B9D2) NP_085055.2:n.215-565_215-564delinsGA
XM_006723405.1:c.89-565_89-564delinsGA (B9D2) XP_006723468.1:n.89-565_89-564delinsGA
XM_011527349.1:c.215-565_215-564delinsGA (B9D2) XP_011525651.1:n.215-565_215-564delinsGA
XM_011527350.1:c.56-565_56-564delinsGA (B9D2) XP_011525652.1:n.56-565_56-564delinsGA
XM_011527349.2:c.215-565_215-564delinsGA (B9D2) XP_011525651.1:n.215-565_215-564delinsGA
XM_011527350.2:c.56-565_56-564delinsGA (B9D2) XP_011525652.1:n.56-565_56-564delinsGA
NM_030578.4:c.215-565_215-564delinsGA (B9D2) MANE Select NP_085055.2:n.215-565_215-564delinsGA