Canonical Allele Identifier: CA2695170512

Gene: F8

Linked Data

• gnomAD v4: X-155022681-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.155022682dup , CM000685.2:g.155022682dup	GRCh38
NC_000023.10:g.154250957dup , CM000685.1:g.154250957dup	GRCh37
NC_000023.9:g.153904151dup	NCBI36
NG_011403.1:g.5042dup
NG_011403.2:g.5042dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.-130dup MANE Select	ENSP00000353393.4:n.-130dup
ENST00000647125.1:c.-130dup	ENSP00000496062.1:n.-130dup
ENST00000360256.8:c.-130dup	ENSP00000353393.4:n.-130dup
ENST00000423959.5:c.38+4098dup	ENSP00000409446.1:n.38+4098dup
ENST00000453950.1:c.39-186dup	ENSP00000389153.1:n.39-186dup
NM_000132.3:c.-130dup	NP_000123.1:n.-130dup
XM_011531126.1:c.38+4098dup	XP_011529428.1:n.38+4098dup
NM_000132.4:c.-130dup MANE Select	NP_000123.1:n.-130dup