Canonical Allele Identifier: CA1139771181

Gene: F8

Linked Data

• gnomAD v4: X-154993261-TTTGTTGTTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154993276_154993284del , CM000685.2:g.154993276_154993284del	GRCh38
NC_000023.10:g.154221551_154221559del , CM000685.1:g.154221551_154221559del	GRCh37
NC_000023.9:g.153874745_153874753del	NCBI36
NG_011403.1:g.34454_34462del
NG_011403.2:g.34454_34462del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.389-122_389-114del MANE Select	ENSP00000353393.4:n.389-122_389-114del
ENST00000647125.1:c.*175-122_*175-114del	ENSP00000496062.1:n.*175-122_*175-114del
ENST00000360256.8:c.389-122_389-114del	ENSP00000353393.4:n.389-122_389-114del
ENST00000423959.5:c.284-122_284-114del	ENSP00000409446.1:n.284-122_284-114del
ENST00000453950.1:c.371-122_371-114del	ENSP00000389153.1:n.371-122_371-114del
NM_000132.3:c.389-122_389-114del	NP_000123.1:n.389-122_389-114del
XM_011531126.1:c.284-122_284-114del	XP_011529428.1:n.284-122_284-114del
NM_000132.4:c.389-122_389-114del MANE Select	NP_000123.1:n.389-122_389-114del