Canonical Allele Identifier: CA792312116

Gene: F11

Linked Data

• dbSNP Id: rs1188745202
• gnomAD v3: 4-186280521-T-TCGGG
• gnomAD v4: 4-186280521-T-TCGGG
• MyVariant Identifiers: chr4:g.187201675_187201676insCGGG (hg19) ; chr4:g.186280521_186280522insCGGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186280521_186280522insCGGG , CM000666.2:g.186280521_186280522insCGGG	GRCh38
NC_000004.11:g.187201675_187201676insCGGG , CM000666.1:g.187201675_187201676insCGGG	GRCh37
NC_000004.10:g.187438669_187438670insCGGG	NCBI36
NG_008051.1:g.19558_19559insCGGG , LRG_583:g.19558_19559insCGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1076_1077insCGGG MANE Select	ENSP00000384957.2:p.Leu360GlyfsTer17
ENST00000264692.8:c.914_915insCGGG	ENSP00000264692.5:p.Leu306GlyfsTer17
ENST00000403665.6:c.1076_1077insCGGG	ENSP00000384957.2:p.Leu360GlyfsTer17
ENST00000452239.1:c.523_524insCGGG
NM_000128.3:c.1076_1077insCGGG , LRG_583t1:c.1076_1077insCGGG	NP_000119.1:p.Leu360GlyfsTer17
XM_005262821.2:c.1079_1080insCGGG	XP_005262878.1:p.Leu361GlyfsTer17
XM_005262822.2:c.1079_1080insCGGG	XP_005262879.1:p.Leu361GlyfsTer17
XM_005262823.2:c.809_810insCGGG	XP_005262880.1:p.Leu271GlyfsTer17
XM_005262824.1:c.1079_1080insCGGG	XP_005262881.1:p.Leu361GlyfsTer17
XM_006714137.1:c.1031_1032insCGGG	XP_006714200.1:p.Leu345GlyfsTer17
XR_938706.1:n.1431_1432insCGGG
XR_938707.1:n.1431_1432insCGGG
XM_005262821.4:c.1079_1080insCGGG	XP_005262878.1:p.Leu361GlyfsTer17
XM_005262822.4:c.1079_1080insCGGG	XP_005262879.1:p.Leu361GlyfsTer17
XM_005262823.4:c.809_810insCGGG	XP_005262880.1:p.Leu271GlyfsTer17
XM_006714137.3:c.1031_1032insCGGG	XP_006714200.1:p.Leu345GlyfsTer17
XM_017007884.2:c.1079_1080insCGGG	XP_016863373.1:p.Leu361GlyfsTer17
XM_017007885.2:c.1079_1080insCGGG	XP_016863374.1:p.Leu361GlyfsTer17
XM_017007886.2:c.1076_1077insCGGG	XP_016863375.1:p.Leu360GlyfsTer17
XR_001741172.2:n.1497_1498insCGGG
NM_000128.4:c.1076_1077insCGGG MANE Select	NP_000119.1:p.Leu360GlyfsTer17