Canonical Allele Identifier: CA2466815673

Gene: F8

Linked Data

• dbSNP Id: rs2072707149

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154863204_154863205insATT , CM000685.2:g.154863204_154863205insATT	GRCh38
NC_000023.10:g.154091479_154091480insATT , CM000685.1:g.154091479_154091480insATT	GRCh37
NC_000023.9:g.153744673_153744674insATT	NCBI36
NG_011403.1:g.164520_164521insATA
NG_011403.2:g.164520_164521insATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6453_6454insATA MANE Select	ENSP00000353393.4:p.Ser2151_Ser2152insIle
ENST00000644698.1:c.186_187insATA	ENSP00000495706.1:p.Ser62_Ser63insIle
ENST00000330287.10:c.48_49insATA	ENSP00000327895.6:p.Ser16_Ser17insIle
ENST00000360256.8:c.6453_6454insATA	ENSP00000353393.4:p.Ser2151_Ser2152insIle
NM_000132.3:c.6453_6454insATA	NP_000123.1:p.Ser2151_Ser2152insIle
NM_019863.2:c.48_49insATA	NP_063916.1:p.Ser16_Ser17insIle
XM_011531126.1:c.6348_6349insATA	XP_011529428.1:p.Ser2116_Ser2117insIle
NM_000132.4:c.6453_6454insATA MANE Select	NP_000123.1:p.Ser2151_Ser2152insIle
NM_019863.3:c.48_49insATA	NP_063916.1:p.Ser16_Ser17insIle