Canonical Allele Identifier: CA2695238517

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.155022406_155022407insC , CM000685.2:g.155022406_155022407insC	GRCh38
NC_000023.10:g.154250681_154250682insC , CM000685.1:g.154250681_154250682insC	GRCh37
NC_000023.9:g.153903875_153903876insC	NCBI36
NG_011403.1:g.5317_5318insG
NG_011403.2:g.5317_5318insG

Transcript Alleles

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