Canonical Allele Identifier: CA2466856485
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154992928_154992933delinsACACTT , CM000685.2:g.154992928_154992933delinsACACTT GRCh38
NC_000023.10:g.154221203_154221208delinsACACTT , CM000685.1:g.154221203_154221208delinsACACTT GRCh37
NC_000023.9:g.153874397_153874402delinsACACTT NCBI36
NG_011403.1:g.34791_34796delinsAAGTGT
NG_011403.2:g.34791_34796delinsAAGTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.601+3_601+8delinsAAGTGT MANE Select ENSP00000353393.4:n.601+3_601+8delinsAAGTGT
ENST00000647125.1:c.*387+3_*387+8delinsAAGTGT ENSP00000496062.1:n.*387+3_*387+8delinsAAGTGT
ENST00000360256.8:c.601+3_601+8delinsAAGTGT ENSP00000353393.4:n.601+3_601+8delinsAAGTGT
ENST00000423959.5:c.496+3_496+8delinsAAGTGT ENSP00000409446.1:n.496+3_496+8delinsAAGTGT
NM_000132.3:c.601+3_601+8delinsAAGTGT NP_000123.1:n.601+3_601+8delinsAAGTGT
XM_011531126.1:c.496+3_496+8delinsAAGTGT XP_011529428.1:n.496+3_496+8delinsAAGTGT
NM_000132.4:c.601+3_601+8delinsAAGTGT MANE Select NP_000123.1:n.601+3_601+8delinsAAGTGT
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