Canonical Allele Identifier: CA2695167413

Gene: F8

Linked Data

• gnomAD v4: X-154837766-GAT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837768_154837769del , CM000685.2:g.154837768_154837769del	GRCh38
NC_000023.10:g.154066043_154066044del , CM000685.1:g.154066043_154066044del	GRCh37
NC_000023.9:g.153719237_153719238del	NCBI36
NG_011403.1:g.189956_189957del
NG_033065.1:g.1895_1896del
NG_011403.2:g.189956_189957del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6901-16_6901-15del MANE Select	ENSP00000353393.4:n.6901-16_6901-15del
ENST00000644698.1:c.634-16_634-15del	ENSP00000495706.1:n.634-16_634-15del
ENST00000330287.10:c.496-16_496-15del	ENSP00000327895.6:n.496-16_496-15del
ENST00000360256.8:c.6901-16_6901-15del	ENSP00000353393.4:n.6901-16_6901-15del
NM_000132.3:c.6901-16_6901-15del	NP_000123.1:n.6901-16_6901-15del
NM_019863.2:c.496-16_496-15del	NP_063916.1:n.496-16_496-15del
XM_011531126.1:c.6796-16_6796-15del	XP_011529428.1:n.6796-16_6796-15del
NM_000132.4:c.6901-16_6901-15del MANE Select	NP_000123.1:n.6901-16_6901-15del
NM_019863.3:c.496-16_496-15del	NP_063916.1:n.496-16_496-15del