Canonical Allele Identifier: CA2507472699

Gene: F8

Linked Data

• gnomAD v4: X-154862957-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154862961del , CM000685.2:g.154862961del	GRCh38
NC_000023.10:g.154091236del , CM000685.1:g.154091236del	GRCh37
NC_000023.9:g.153744430del	NCBI36
NG_011403.1:g.164766del
NG_011403.2:g.164766del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6574+125del MANE Select	ENSP00000353393.4:n.6574+125del
ENST00000644698.1:c.307+125del	ENSP00000495706.1:n.307+125del
ENST00000330287.10:c.169+125del	ENSP00000327895.6:n.169+125del
ENST00000360256.8:c.6574+125del	ENSP00000353393.4:n.6574+125del
NM_000132.3:c.6574+125del	NP_000123.1:n.6574+125del
NM_019863.2:c.169+125del	NP_063916.1:n.169+125del
XM_011531126.1:c.6469+125del	XP_011529428.1:n.6469+125del
NM_000132.4:c.6574+125del MANE Select	NP_000123.1:n.6574+125del
NM_019863.3:c.169+125del	NP_063916.1:n.169+125del