Canonical Allele Identifier: CA2466814950

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154860389_154860390delinsAT , CM000685.2:g.154860389_154860390delinsAT	GRCh38
NC_000023.10:g.154088664_154088665delinsAT , CM000685.1:g.154088664_154088665delinsAT	GRCh37
NC_000023.9:g.153741858_153741859delinsAT	NCBI36
NG_011403.1:g.167334_167335delinsAT
NG_011403.2:g.167334_167335delinsAT

Transcript Alleles

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