Canonical Allele Identifier: CA2672903862

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186287609_186287610insATGTAT , CM000666.2:g.186287609_186287610insATGTAT GRCh38
NC_000004.11:g.187208763_187208764insATGTAT , CM000666.1:g.187208763_187208764insATGTAT GRCh37
NC_000004.10:g.187445757_187445758insATGTAT NCBI36
NG_008051.1:g.26646_26647insATGTAT , LRG_583:g.26646_26647insATGTAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.7:c.1577-75_1577-74insATGTAT (F11) MANE Select ENSP00000384957.2:n.1577-75_1577-74insATGTAT
ENST00000264691.4:c.177-75_177-74insATGTAT (F11)
ENST00000264692.8:c.1415-75_1415-74insATGTAT (F11) ENSP00000264692.5:n.1415-75_1415-74insATGTAT
ENST00000403665.6:c.1577-75_1577-74insATGTAT (F11) ENSP00000384957.2:n.1577-75_1577-74insATGTAT
ENST00000503841.1:n.21_22insATGTAT (F11)
NM_000128.3:c.1577-75_1577-74insATGTAT , LRG_583t1:c.1577-75_1577-74insATGTAT (F11) NP_000119.1:n.1577-75_1577-74insATGTAT
NR_033900.1:n.1066+821_1066+822insCATATA (F11-AS1)
XM_005262821.2:c.1580-75_1580-74insATGTAT (F11) XP_005262878.1:n.1580-75_1580-74insATGTAT
XM_005262822.2:c.1484-75_1484-74insATGTAT (F11) XP_005262879.1:n.1484-75_1484-74insATGTAT
XM_005262823.2:c.1310-75_1310-74insATGTAT (F11) XP_005262880.1:n.1310-75_1310-74insATGTAT
XM_006714137.1:c.1532-75_1532-74insATGTAT (F11) XP_006714200.1:n.1532-75_1532-74insATGTAT
XR_938706.1:n.1985-75_1985-74insATGTAT (F11)
XR_938707.1:n.1889-75_1889-74insATGTAT (F11)
XM_005262821.4:c.1580-75_1580-74insATGTAT (F11) XP_005262878.1:n.1580-75_1580-74insATGTAT
XM_005262822.4:c.1484-75_1484-74insATGTAT (F11) XP_005262879.1:n.1484-75_1484-74insATGTAT
XM_005262823.4:c.1310-75_1310-74insATGTAT (F11) XP_005262880.1:n.1310-75_1310-74insATGTAT
XM_006714137.3:c.1532-75_1532-74insATGTAT (F11) XP_006714200.1:n.1532-75_1532-74insATGTAT
NM_000128.4:c.1577-75_1577-74insATGTAT (F11) MANE Select NP_000119.1:n.1577-75_1577-74insATGTAT