Canonical Allele Identifier: CA645237062

Gene: F8

Linked Data

• dbSNP Id: rs1557271067
• gnomAD v2: X-154066032-A-AAGAGGAAAGATAGCATTT
• gnomAD v4: X-154837757-A-AAGAGGAAAGATAGCATTT
• MyVariant Identifiers: chrX:g.154066032_154066033insAGAGGAAAGATAGCATTT (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837759_154837776dup , CM000685.2:g.154837759_154837776dup	GRCh38
NC_000023.10:g.154066034_154066051dup , CM000685.1:g.154066034_154066051dup	GRCh37
NC_000023.9:g.153719228_153719245dup	NCBI36
NG_011403.1:g.189949_189966dup
NG_033065.1:g.1888_1905dup
NG_011403.2:g.189949_189966dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6901-23_6901-6dup MANE Select	ENSP00000353393.4:n.6901-23_6901-6dup
ENST00000644698.1:c.634-23_634-6dup	ENSP00000495706.1:n.634-23_634-6dup
ENST00000330287.10:c.496-23_496-6dup	ENSP00000327895.6:n.496-23_496-6dup
ENST00000360256.8:c.6901-23_6901-6dup	ENSP00000353393.4:n.6901-23_6901-6dup
NM_000132.3:c.6901-23_6901-6dup	NP_000123.1:n.6901-23_6901-6dup
NM_019863.2:c.496-23_496-6dup	NP_063916.1:n.496-23_496-6dup
XM_011531126.1:c.6796-23_6796-6dup	XP_011529428.1:n.6796-23_6796-6dup
NM_000132.4:c.6901-23_6901-6dup MANE Select	NP_000123.1:n.6901-23_6901-6dup
NM_019863.3:c.496-23_496-6dup	NP_063916.1:n.496-23_496-6dup