Canonical Allele Identifier: CA2695238518

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.155022406_155022407insA , CM000685.2:g.155022406_155022407insA	GRCh38
NC_000023.10:g.154250681_154250682insA , CM000685.1:g.154250681_154250682insA	GRCh37
NC_000023.9:g.153903875_153903876insA	NCBI36
NG_011403.1:g.5317_5318insT
NG_011403.2:g.5317_5318insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.143+3_143+4insT MANE Select	ENSP00000353393.4:n.143+3_143+4insT
ENST00000647125.1:c.121+25_121+26insT	ENSP00000496062.1:n.121+25_121+26insT
ENST00000360256.8:c.143+3_143+4insT	ENSP00000353393.4:n.143+3_143+4insT
ENST00000423959.5:c.38+4373_38+4374insT	ENSP00000409446.1:n.38+4373_38+4374insT
ENST00000453950.1:c.125+3_125+4insT	ENSP00000389153.1:n.125+3_125+4insT
NM_000132.3:c.143+3_143+4insT	NP_000123.1:n.143+3_143+4insT
XM_011531126.1:c.38+4373_38+4374insT	XP_011529428.1:n.38+4373_38+4374insT
NM_000132.4:c.143+3_143+4insT MANE Select	NP_000123.1:n.143+3_143+4insT