Canonical Allele Identifier: CA2695170256

Gene: F8

Linked Data

• gnomAD v4: X-154997168-GAGTCAAGGTCAC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154997172_154997183del , CM000685.2:g.154997172_154997183del	GRCh38
NC_000023.10:g.154225447_154225458del , CM000685.1:g.154225447_154225458del	GRCh37
NC_000023.9:g.153878641_153878652del	NCBI36
NG_011403.1:g.30544_30555del
NG_011403.2:g.30544_30555del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.266-85_266-74del MANE Select	ENSP00000353393.4:n.266-85_266-74del
ENST00000647125.1:c.*52-85_*52-74del	ENSP00000496062.1:n.*52-85_*52-74del
ENST00000360256.8:c.266-85_266-74del	ENSP00000353393.4:n.266-85_266-74del
ENST00000423959.5:c.161-85_161-74del	ENSP00000409446.1:n.161-85_161-74del
ENST00000453950.1:c.248-85_248-74del	ENSP00000389153.1:n.248-85_248-74del
NM_000132.3:c.266-85_266-74del	NP_000123.1:n.266-85_266-74del
XM_011531126.1:c.161-85_161-74del	XP_011529428.1:n.161-85_161-74del
NM_000132.4:c.266-85_266-74del MANE Select	NP_000123.1:n.266-85_266-74del