Canonical Allele Identifier: CA2500170773

Gene: FYB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.56777976_56777977insTACGGCG , CM000663.2:g.56777976_56777977insTACGGCG	GRCh38
NC_000001.10:g.57243649_57243650insTACGGCG , CM000663.1:g.57243649_57243650insTACGGCG	GRCh37
NC_000001.9:g.57016237_57016238insTACGGCG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343433.7:c.953+9198_953+9199insCGCCGTA MANE Select	ENSP00000345972.6:n.953+9198_953+9199insCGCCGTA
ENST00000343433.6:c.953+9198_953+9199insCGCCGTA	ENSP00000345972.6:n.953+9198_953+9199insCGCCGTA
ENST00000484327.1:n.1359+9198_1359+9199insCGCCGTA
NM_001004303.4:c.953+9198_953+9199insCGCCGTA	NP_001004303.3:n.953+9198_953+9199insCGCCGTA
XM_005270584.3:c.953+9198_953+9199insCGCCGTA	XP_005270641.1:n.953+9198_953+9199insCGCCGTA
XM_011540898.1:c.953+9198_953+9199insCGCCGTA	XP_011539200.1:n.953+9198_953+9199insCGCCGTA
XM_011540899.1:c.953+9198_953+9199insCGCCGTA	XP_011539201.1:n.953+9198_953+9199insCGCCGTA
XM_011540900.1:c.953+9198_953+9199insCGCCGTA	XP_011539202.1:n.953+9198_953+9199insCGCCGTA
XM_011540901.1:c.953+9198_953+9199insCGCCGTA	XP_011539203.1:n.953+9198_953+9199insCGCCGTA
XM_011540902.1:c.953+9198_953+9199insCGCCGTA	XP_011539204.1:n.953+9198_953+9199insCGCCGTA
XM_011540903.1:c.953+9198_953+9199insCGCCGTA	XP_011539205.1:n.953+9198_953+9199insCGCCGTA
XM_011540905.1:c.953+9198_953+9199insCGCCGTA	XP_011539207.1:n.953+9198_953+9199insCGCCGTA
XM_011540907.1:c.953+9198_953+9199insCGCCGTA	XP_011539209.1:n.953+9198_953+9199insCGCCGTA
XR_946569.1:n.1359+9198_1359+9199insCGCCGTA
XR_946570.1:n.1359+9198_1359+9199insCGCCGTA
XR_946571.1:n.1359+9198_1359+9199insCGCCGTA
XR_946572.1:n.1359+9198_1359+9199insCGCCGTA
XM_011540900.2:c.953+9198_953+9199insCGCCGTA	XP_011539202.1:n.953+9198_953+9199insCGCCGTA
XM_011540903.2:c.953+9198_953+9199insCGCCGTA	XP_011539205.1:n.953+9198_953+9199insCGCCGTA
XM_011540905.2:c.953+9198_953+9199insCGCCGTA	XP_011539207.1:n.953+9198_953+9199insCGCCGTA
XM_017000544.2:c.563+9198_563+9199insCGCCGTA	XP_016856033.1:n.563+9198_563+9199insCGCCGTA
XM_017000545.1:c.563+9198_563+9199insCGCCGTA	XP_016856034.1:n.563+9198_563+9199insCGCCGTA
XM_017000548.1:c.953+9198_953+9199insCGCCGTA	XP_016856037.1:n.953+9198_953+9199insCGCCGTA
XM_024453853.1:c.953+9198_953+9199insCGCCGTA	XP_024309621.1:n.953+9198_953+9199insCGCCGTA
XR_001737026.1:n.1359+9198_1359+9199insCGCCGTA
XR_946572.2:n.1359+9198_1359+9199insCGCCGTA
NM_001004303.5:c.953+9198_953+9199insCGCCGTA MANE Select	NP_001004303.3:n.953+9198_953+9199insCGCCGTA