Canonical Allele Identifier: CA557055335

Gene: F11

Linked Data

• gnomAD v2: 4-187205778-T-TGTGG
• MyVariant Identifiers: chr4:g.187205778_187205779insGTGG (hg19) ; chr4:g.186284624_186284625insGTGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284627_186284628insGGTG , CM000666.2:g.186284627_186284628insGGTG	GRCh38
NC_000004.11:g.187205781_187205782insGGTG , CM000666.1:g.187205781_187205782insGGTG	GRCh37
NC_000004.10:g.187442775_187442776insGGTG	NCBI36
NG_008051.1:g.23664_23665insGGTG , LRG_583:g.23664_23665insGGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1304+367_1304+368insGGTG MANE Select	ENSP00000384957.2:n.1304+367_1304+368insGGTG
ENST00000264692.8:c.1142+367_1142+368insGGTG	ENSP00000264692.5:n.1142+367_1142+368insGGTG
ENST00000403665.6:c.1304+367_1304+368insGGTG	ENSP00000384957.2:n.1304+367_1304+368insGGTG
NM_000128.3:c.1304+367_1304+368insGGTG , LRG_583t1:c.1304+367_1304+368insGGTG	NP_000119.1:n.1304+367_1304+368insGGTG
XM_005262821.2:c.1307+367_1307+368insGGTG	XP_005262878.1:n.1307+367_1307+368insGGTG
XM_005262822.2:c.1307+367_1307+368insGGTG	XP_005262879.1:n.1307+367_1307+368insGGTG
XM_005262823.2:c.1037+367_1037+368insGGTG	XP_005262880.1:n.1037+367_1037+368insGGTG
XM_005262824.1:c.1307+367_1307+368insGGTG	XP_005262881.1:n.1307+367_1307+368insGGTG
XM_006714137.1:c.1259+367_1259+368insGGTG	XP_006714200.1:n.1259+367_1259+368insGGTG
XR_938706.1:n.1712+367_1712+368insGGTG
XR_938707.1:n.1712+367_1712+368insGGTG
XM_005262821.4:c.1307+367_1307+368insGGTG	XP_005262878.1:n.1307+367_1307+368insGGTG
XM_005262822.4:c.1307+367_1307+368insGGTG	XP_005262879.1:n.1307+367_1307+368insGGTG
XM_005262823.4:c.1037+367_1037+368insGGTG	XP_005262880.1:n.1037+367_1037+368insGGTG
XM_006714137.3:c.1259+367_1259+368insGGTG	XP_006714200.1:n.1259+367_1259+368insGGTG
XR_001741172.2:n.1778+367_1778+368insGGTG
NM_000128.4:c.1304+367_1304+368insGGTG MANE Select	NP_000119.1:n.1304+367_1304+368insGGTG