Canonical Allele Identifier: CA2695237181

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154863202_154863203delinsATAT , CM000685.2:g.154863202_154863203delinsATAT	GRCh38
NC_000023.10:g.154091477_154091478delinsATAT , CM000685.1:g.154091477_154091478delinsATAT	GRCh37
NC_000023.9:g.153744671_153744672delinsATAT	NCBI36
NG_011403.1:g.164521_164522delinsATAT
NG_011403.2:g.164521_164522delinsATAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.6454_6455delinsATAT MANE Select	ENSP00000353393.4:p.Ser2152IlefsTer4
ENST00000644698.1:c.187_188delinsATAT	ENSP00000495706.1:p.Ser63IlefsTer4
ENST00000330287.10:c.49_50delinsATAT	ENSP00000327895.6:p.Ser17IlefsTer4
ENST00000360256.8:c.6454_6455delinsATAT	ENSP00000353393.4:p.Ser2152IlefsTer4
NM_000132.3:c.6454_6455delinsATAT	NP_000123.1:p.Ser2152IlefsTer4
NM_019863.2:c.49_50delinsATAT	NP_063916.1:p.Ser17IlefsTer4
XM_011531126.1:c.6349_6350delinsATAT	XP_011529428.1:p.Ser2117IlefsTer4
NM_000132.4:c.6454_6455delinsATAT MANE Select	NP_000123.1:p.Ser2152IlefsTer4
NM_019863.3:c.49_50delinsATAT	NP_063916.1:p.Ser17IlefsTer4