Canonical Allele Identifier: CA2830563606

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154905085_154905086insAGAAGA , CM000685.2:g.154905085_154905086insAGAAGA	GRCh38
NC_000023.10:g.154133360_154133361insAGAAGA , CM000685.1:g.154133360_154133361insAGAAGA	GRCh37
NC_000023.9:g.153786554_153786555insAGAAGA	NCBI36
NG_011403.1:g.122638_122639insTCTTCT
NG_011403.2:g.122638_122639insTCTTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5374-63_5374-62insTCTTCT MANE Select	ENSP00000353393.4:n.5374-63_5374-62insTCTTCT
ENST00000360256.8:c.5374-63_5374-62insTCTTCT	ENSP00000353393.4:n.5374-63_5374-62insTCTTCT
NM_000132.3:c.5374-63_5374-62insTCTTCT	NP_000123.1:n.5374-63_5374-62insTCTTCT
XM_011531126.1:c.5269-63_5269-62insTCTTCT	XP_011529428.1:n.5269-63_5269-62insTCTTCT
NM_000132.4:c.5374-63_5374-62insTCTTCT MANE Select	NP_000123.1:n.5374-63_5374-62insTCTTCT