Canonical Allele Identifier: CA2695167713

Gene: F8

Linked Data

• gnomAD v4: X-154860389-A-ATTCT

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154860391_154860392insCTTT , CM000685.2:g.154860391_154860392insCTTT	GRCh38
NC_000023.10:g.154088666_154088667insCTTT , CM000685.1:g.154088666_154088667insCTTT	GRCh37
NC_000023.9:g.153741860_153741861insCTTT	NCBI36
NG_011403.1:g.167334_167335insAGAA
NG_011403.2:g.167334_167335insAGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6900+42_6900+43insAGAA MANE Select	ENSP00000353393.4:n.6900+42_6900+43insAGAA
ENST00000644698.1:c.633+42_633+43insAGAA	ENSP00000495706.1:n.633+42_633+43insAGAA
ENST00000330287.10:c.495+42_495+43insAGAA	ENSP00000327895.6:n.495+42_495+43insAGAA
ENST00000360256.8:c.6900+42_6900+43insAGAA	ENSP00000353393.4:n.6900+42_6900+43insAGAA
NM_000132.3:c.6900+42_6900+43insAGAA	NP_000123.1:n.6900+42_6900+43insAGAA
NM_019863.2:c.495+42_495+43insAGAA	NP_063916.1:n.495+42_495+43insAGAA
XM_011531126.1:c.6795+42_6795+43insAGAA	XP_011529428.1:n.6795+42_6795+43insAGAA
NM_000132.4:c.6900+42_6900+43insAGAA MANE Select	NP_000123.1:n.6900+42_6900+43insAGAA
NM_019863.3:c.495+42_495+43insAGAA	NP_063916.1:n.495+42_495+43insAGAA