Canonical Allele Identifier: CA2466835653

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154928340_154928341delinsCT , CM000685.2:g.154928340_154928341delinsCT	GRCh38
NC_000023.10:g.154156615_154156616delinsCT , CM000685.1:g.154156615_154156616delinsCT	GRCh37
NC_000023.9:g.153809809_153809810delinsCT	NCBI36
NG_011403.1:g.99383_99384delinsAG
NG_011403.2:g.99383_99384delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5219+230_5219+231delinsAG MANE Select	ENSP00000353393.4:n.5219+230_5219+231delinsAG
ENST00000360256.8:c.5219+230_5219+231delinsAG	ENSP00000353393.4:n.5219+230_5219+231delinsAG
NM_000132.3:c.5219+230_5219+231delinsAG	NP_000123.1:n.5219+230_5219+231delinsAG
XM_011531126.1:c.5114+230_5114+231delinsAG	XP_011529428.1:n.5114+230_5114+231delinsAG
NM_000132.4:c.5219+230_5219+231delinsAG MANE Select	NP_000123.1:n.5219+230_5219+231delinsAG