Canonical Allele Identifier: CA2466814962

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154860411_154860415delinsTTTCC , CM000685.2:g.154860411_154860415delinsTTTCC	GRCh38
NC_000023.10:g.154088686_154088690delinsTTTCC , CM000685.1:g.154088686_154088690delinsTTTCC	GRCh37
NC_000023.9:g.153741880_153741884delinsTTTCC	NCBI36
NG_011403.1:g.167309_167313delinsGGAAA
NG_011403.2:g.167309_167313delinsGGAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6900+17_6900+21delinsGGAAA MANE Select	ENSP00000353393.4:n.6900+17_6900+21delinsGGAAA
ENST00000644698.1:c.633+17_633+21delinsGGAAA	ENSP00000495706.1:n.633+17_633+21delinsGGAAA
ENST00000330287.10:c.495+17_495+21delinsGGAAA	ENSP00000327895.6:n.495+17_495+21delinsGGAAA
ENST00000360256.8:c.6900+17_6900+21delinsGGAAA	ENSP00000353393.4:n.6900+17_6900+21delinsGGAAA
NM_000132.3:c.6900+17_6900+21delinsGGAAA	NP_000123.1:n.6900+17_6900+21delinsGGAAA
NM_019863.2:c.495+17_495+21delinsGGAAA	NP_063916.1:n.495+17_495+21delinsGGAAA
XM_011531126.1:c.6795+17_6795+21delinsGGAAA	XP_011529428.1:n.6795+17_6795+21delinsGGAAA
NM_000132.4:c.6900+17_6900+21delinsGGAAA MANE Select	NP_000123.1:n.6900+17_6900+21delinsGGAAA
NM_019863.3:c.495+17_495+21delinsGGAAA	NP_063916.1:n.495+17_495+21delinsGGAAA