Canonical Allele Identifier: CA1217904113

Gene: F13B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197039087_197039098delinsATATAGTCTAGT , CM000663.2:g.197039087_197039098delinsATATAGTCTAGT	GRCh38
NC_000001.10:g.197008217_197008228delinsATATAGTCTAGT , CM000663.1:g.197008217_197008228delinsATATAGTCTAGT	GRCh37
NC_000001.9:g.195274840_195274851delinsATATAGTCTAGT	NCBI36
NG_012065.1:g.33170_33181delinsACTAGACTATAT , LRG_550:g.33170_33181delinsACTAGACTATAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367412.2:c.*280_*291delinsACTAGACTATAT MANE Select	ENSP00000356382.2:n.*280_*291delinsACTAGACTATAT
ENST00000649282.1:c.1021_1032delinsACTAGACTATAT	ENSP00000497116.1:n.1021_1032delinsACTAGACTATAT
XM_011509283.2:c.*1201_*1212delinsACTAGACTATAT	XP_011507585.1:n.*1201_*1212delinsACTAGACTATAT
XM_011509284.2:c.*1201_*1212delinsACTAGACTATAT	XP_011507586.1:n.*1201_*1212delinsACTAGACTATAT
XM_011509286.2:c.*1201_*1212delinsACTAGACTATAT	XP_011507588.1:n.*1201_*1212delinsACTAGACTATAT
NM_001994.3:c.*280_*291delinsACTAGACTATAT MANE Select	NP_001985.2:n.*280_*291delinsACTAGACTATAT