Canonical Allele Identifier: CA2824314863

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154904159_154904160insCCAAACACACCCA , CM000685.2:g.154904159_154904160insCCAAACACACCCA	GRCh38
NC_000023.10:g.154132434_154132435insCCAAACACACCCA , CM000685.1:g.154132434_154132435insCCAAACACACCCA	GRCh37
NC_000023.9:g.153785628_153785629insCCAAACACACCCA	NCBI36
NG_011403.1:g.123565_123566insGGGTGTGTTTGGT
NG_011403.2:g.123565_123566insGGGTGTGTTTGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5816-71_5816-70insGGGTGTGTTTGGT MANE Select	ENSP00000353393.4:n.5816-71_5816-70insGGGTGTGTTTGGT
ENST00000360256.8:c.5816-71_5816-70insGGGTGTGTTTGGT	ENSP00000353393.4:n.5816-71_5816-70insGGGTGTGTTTGGT
NM_000132.3:c.5816-71_5816-70insGGGTGTGTTTGGT	NP_000123.1:n.5816-71_5816-70insGGGTGTGTTTGGT
XM_011531126.1:c.5711-71_5711-70insGGGTGTGTTTGGT	XP_011529428.1:n.5711-71_5711-70insGGGTGTGTTTGGT
NM_000132.4:c.5816-71_5816-70insGGGTGTGTTTGGT MANE Select	NP_000123.1:n.5816-71_5816-70insGGGTGTGTTTGGT