Canonical Allele Identifier: CA2695152097

Gene: F8

Linked Data

• gnomAD v4: X-154896318-CTA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154896319_154896320del , CM000685.2:g.154896319_154896320del	GRCh38
NC_000023.10:g.154124594_154124595del , CM000685.1:g.154124594_154124595del	GRCh37
NC_000023.9:g.153777788_153777789del	NCBI36
NG_011403.1:g.131404_131405del
NG_011403.2:g.131404_131405del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6274-88_6274-87del MANE Select	ENSP00000353393.4:n.6274-88_6274-87del
ENST00000360256.8:c.6274-88_6274-87del	ENSP00000353393.4:n.6274-88_6274-87del
NM_000132.3:c.6274-88_6274-87del	NP_000123.1:n.6274-88_6274-87del
XM_011531126.1:c.6169-88_6169-87del	XP_011529428.1:n.6169-88_6169-87del
NM_000132.4:c.6274-88_6274-87del MANE Select	NP_000123.1:n.6274-88_6274-87del