Canonical Allele Identifier: CA2695237174

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154863171_154863172delinsACATC , CM000685.2:g.154863171_154863172delinsACATC	GRCh38
NC_000023.10:g.154091446_154091447delinsACATC , CM000685.1:g.154091446_154091447delinsACATC	GRCh37
NC_000023.9:g.153744640_153744641delinsACATC	NCBI36
NG_011403.1:g.164552_164553delinsGATGT
NG_011403.2:g.164552_164553delinsGATGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.6485_6486delinsGATGT MANE Select	ENSP00000353393.4:p.Pro2162delinsArgCys
ENST00000644698.1:c.218_219delinsGATGT	ENSP00000495706.1:p.Pro73delinsArgCys
ENST00000330287.10:c.80_81delinsGATGT	ENSP00000327895.6:p.Pro27delinsArgCys
ENST00000360256.8:c.6485_6486delinsGATGT	ENSP00000353393.4:p.Pro2162delinsArgCys
NM_000132.3:c.6485_6486delinsGATGT	NP_000123.1:p.Pro2162delinsArgCys
NM_019863.2:c.80_81delinsGATGT	NP_063916.1:p.Pro27delinsArgCys
XM_011531126.1:c.6380_6381delinsGATGT	XP_011529428.1:p.Pro2127delinsArgCys
NM_000132.4:c.6485_6486delinsGATGT MANE Select	NP_000123.1:p.Pro2162delinsArgCys
NM_019863.3:c.80_81delinsGATGT	NP_063916.1:p.Pro27delinsArgCys