Canonical Allele Identifier: CA2649657755

Gene: F13B

Linked Data

• gnomAD v4: 1-197039235-C-CCAATAAATAAT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197039235_197039236insCAATAAATAAT , CM000663.2:g.197039235_197039236insCAATAAATAAT	GRCh38
NC_000001.10:g.197008365_197008366insCAATAAATAAT , CM000663.1:g.197008365_197008366insCAATAAATAAT	GRCh37
NC_000001.9:g.195274988_195274989insCAATAAATAAT	NCBI36
NG_012065.1:g.33032_33033insATTATTTATTG , LRG_550:g.33032_33033insATTATTTATTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367412.2:c.*142_*143insATTATTTATTG MANE Select	ENSP00000356382.2:n.*142_*143insATTATTTATTG
ENST00000649282.1:c.883_884insATTATTTATTG	ENSP00000497116.1:n.883_884insATTATTTATTG
ENST00000367412.1:c.*142_*143insATTATTTATTG	ENSP00000356382.1:n.*142_*143insATTATTTATTG
NM_001994.2:c.*142_*143insATTATTTATTG , LRG_550t1:c.*142_*143insATTATTTATTG	NP_001985.2:n.*142_*143insATTATTTATTG
XM_011509283.2:c.*1063_*1064insATTATTTATTG	XP_011507585.1:n.*1063_*1064insATTATTTATTG
XM_011509284.2:c.*1063_*1064insATTATTTATTG	XP_011507586.1:n.*1063_*1064insATTATTTATTG
XM_011509286.2:c.*1063_*1064insATTATTTATTG	XP_011507588.1:n.*1063_*1064insATTATTTATTG
NM_001994.3:c.*142_*143insATTATTTATTG MANE Select	NP_001985.2:n.*142_*143insATTATTTATTG