Canonical Allele Identifier: CA2695170254

Gene: F8

Linked Data

• gnomAD v4: X-154997166-T-TAGAGTC

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154997168_154997173dup , CM000685.2:g.154997168_154997173dup	GRCh38
NC_000023.10:g.154225443_154225448dup , CM000685.1:g.154225443_154225448dup	GRCh37
NC_000023.9:g.153878637_153878642dup	NCBI36
NG_011403.1:g.30552_30557dup
NG_011403.2:g.30552_30557dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.266-77_266-72dup MANE Select	ENSP00000353393.4:n.266-77_266-72dup
ENST00000647125.1:c.*52-77_*52-72dup	ENSP00000496062.1:n.*52-77_*52-72dup
ENST00000360256.8:c.266-77_266-72dup	ENSP00000353393.4:n.266-77_266-72dup
ENST00000423959.5:c.161-77_161-72dup	ENSP00000409446.1:n.161-77_161-72dup
ENST00000453950.1:c.248-77_248-72dup	ENSP00000389153.1:n.248-77_248-72dup
NM_000132.3:c.266-77_266-72dup	NP_000123.1:n.266-77_266-72dup
XM_011531126.1:c.161-77_161-72dup	XP_011529428.1:n.161-77_161-72dup
NM_000132.4:c.266-77_266-72dup MANE Select	NP_000123.1:n.266-77_266-72dup