Canonical Allele Identifier: CA2536470690

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169530727_169530728insCA , CM000663.2:g.169530727_169530728insCA	GRCh38
NC_000001.10:g.169499965_169499966insCA , CM000663.1:g.169499965_169499966insCA	GRCh37
NC_000001.9:g.167766589_167766590insCA	NCBI36
NG_011806.1:g.60804_60805insTG , LRG_553:g.60804_60805insTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000367797.9:c.5208+58_5208+59insTG MANE Select	ENSP00000356771.3:n.5208+58_5208+59insTG
ENST00000367796.3:c.5223+58_5223+59insTG	ENSP00000356770.3:n.5223+58_5223+59insTG
ENST00000367797.7:c.5208+58_5208+59insTG	ENSP00000356771.3:n.5208+58_5208+59insTG
NM_000130.4:c.5208+58_5208+59insTG , LRG_553t1:c.5208+58_5208+59insTG	NP_000121.2:n.5208+58_5208+59insTG
XM_017000660.2:c.4797+58_4797+59insTG	XP_016856149.1:n.4797+58_4797+59insTG
NM_000130.5:c.5208+58_5208+59insTG MANE Select	NP_000121.2:n.5208+58_5208+59insTG