Canonical Allele Identifier: CA2695167276
Gene: F8 HGNC NCBI

Linked Data

gnomAD v4: X-154837401-GAGTTA-G
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154837408_154837412del , CM000685.2:g.154837408_154837412del GRCh38
NC_000023.10:g.154065683_154065687del , CM000685.1:g.154065683_154065687del GRCh37
NC_000023.9:g.153718877_153718881del NCBI36
NG_011403.1:g.190318_190322del
NG_033065.1:g.2257_2261del
NG_011403.2:g.190318_190322del

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.*191_*195del MANE Select ENSP00000353393.4:n.*191_*195del
ENST00000644698.1:c.*191_*195del ENSP00000495706.1:n.*191_*195del
ENST00000330287.10:c.*191_*195del ENSP00000327895.6:n.*191_*195del
ENST00000360256.8:c.*191_*195del ENSP00000353393.4:n.*191_*195del
NM_000132.3:c.*191_*195del NP_000123.1:n.*191_*195del
NM_019863.2:c.*191_*195del NP_063916.1:n.*191_*195del
XM_011531126.1:c.*191_*195del XP_011529428.1:n.*191_*195del
NM_000132.4:c.*191_*195del MANE Select NP_000123.1:n.*191_*195del
NM_019863.3:c.*191_*195del NP_063916.1:n.*191_*195del
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