Canonical Allele Identifier: CA1206144051

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169549634_169549637delinsCAAA , CM000663.2:g.169549634_169549637delinsCAAA	GRCh38
NC_000001.10:g.169518872_169518875delinsCAAA , CM000663.1:g.169518872_169518875delinsCAAA	GRCh37
NC_000001.9:g.167785496_167785499delinsCAAA	NCBI36
NG_011806.1:g.41895_41898delinsTTTG , LRG_553:g.41895_41898delinsTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.1611+164_1611+167delinsTTTG MANE Select	ENSP00000356771.3:n.1611+164_1611+167delinsTTTG
ENST00000367796.3:c.1611+164_1611+167delinsTTTG	ENSP00000356770.3:n.1611+164_1611+167delinsTTTG
ENST00000367797.7:c.1611+164_1611+167delinsTTTG	ENSP00000356771.3:n.1611+164_1611+167delinsTTTG
NM_000130.4:c.1611+164_1611+167delinsTTTG , LRG_553t1:c.1611+164_1611+167delinsTTTG	NP_000121.2:n.1611+164_1611+167delinsTTTG
XM_017000660.2:c.1200+164_1200+167delinsTTTG	XP_016856149.1:n.1200+164_1200+167delinsTTTG
NM_000130.5:c.1611+164_1611+167delinsTTTG MANE Select	NP_000121.2:n.1611+164_1611+167delinsTTTG