Canonical Allele Identifier: CA645251877

Gene: F8

Linked Data

• dbSNP Id: rs1557287637
• gnomAD v2: X-154250939-C-CAATGTTA
• gnomAD v3: X-155022664-C-CAATGTTA
• gnomAD v4: X-155022664-C-CAATGTTA
• MyVariant Identifiers: chrX:g.154250939_154250940insAATGTTA (hg19) ; chrX:g.155022664_155022665insAATGTTA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.155022664_155022665insAATGTTA , CM000685.2:g.155022664_155022665insAATGTTA	GRCh38
NC_000023.10:g.154250939_154250940insAATGTTA , CM000685.1:g.154250939_154250940insAATGTTA	GRCh37
NC_000023.9:g.153904133_153904134insAATGTTA	NCBI36
NG_011403.1:g.5059_5060insTAACATT
NG_011403.2:g.5059_5060insTAACATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.-113_-112insTAACATT MANE Select	ENSP00000353393.4:n.-113_-112insTAACATT
ENST00000647125.1:c.-113_-112insTAACATT	ENSP00000496062.1:n.-113_-112insTAACATT
ENST00000360256.8:c.-113_-112insTAACATT	ENSP00000353393.4:n.-113_-112insTAACATT
ENST00000423959.5:c.38+4115_38+4116insTAACATT	ENSP00000409446.1:n.38+4115_38+4116insTAACATT
ENST00000453950.1:c.39-169_39-168insTAACATT	ENSP00000389153.1:n.39-169_39-168insTAACATT
NM_000132.3:c.-113_-112insTAACATT	NP_000123.1:n.-113_-112insTAACATT
XM_011531126.1:c.38+4115_38+4116insTAACATT	XP_011529428.1:n.38+4115_38+4116insTAACATT
NM_000132.4:c.-113_-112insTAACATT MANE Select	NP_000123.1:n.-113_-112insTAACATT