Canonical Allele Identifier: CA2466814955

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154860397_154860398delinsTC , CM000685.2:g.154860397_154860398delinsTC	GRCh38
NC_000023.10:g.154088672_154088673delinsTC , CM000685.1:g.154088672_154088673delinsTC	GRCh37
NC_000023.9:g.153741866_153741867delinsTC	NCBI36
NG_011403.1:g.167326_167327delinsGA
NG_011403.2:g.167326_167327delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6900+34_6900+35delinsGA MANE Select	ENSP00000353393.4:n.6900+34_6900+35delinsGA
ENST00000644698.1:c.633+34_633+35delinsGA	ENSP00000495706.1:n.633+34_633+35delinsGA
ENST00000330287.10:c.495+34_495+35delinsGA	ENSP00000327895.6:n.495+34_495+35delinsGA
ENST00000360256.8:c.6900+34_6900+35delinsGA	ENSP00000353393.4:n.6900+34_6900+35delinsGA
NM_000132.3:c.6900+34_6900+35delinsGA	NP_000123.1:n.6900+34_6900+35delinsGA
NM_019863.2:c.495+34_495+35delinsGA	NP_063916.1:n.495+34_495+35delinsGA
XM_011531126.1:c.6795+34_6795+35delinsGA	XP_011529428.1:n.6795+34_6795+35delinsGA
NM_000132.4:c.6900+34_6900+35delinsGA MANE Select	NP_000123.1:n.6900+34_6900+35delinsGA
NM_019863.3:c.495+34_495+35delinsGA	NP_063916.1:n.495+34_495+35delinsGA