Canonical Allele Identifier: CA442640149

Gene: F11

Linked Data

• gnomAD v4: 4-186285767-G-C
• MyVariant Identifiers: chr4:g.187206921G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285767G>C , CM000666.2:g.186285767G>C	GRCh38
NC_000004.11:g.187206921G>C , CM000666.1:g.187206921G>C	GRCh37
NC_000004.10:g.187443915G>C	NCBI36
NG_008051.1:g.24804G>C , LRG_583:g.24804G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1434G>C MANE Select	ENSP00000384957.2:p.Gly478=
ENST00000264691.4:c.130G>C
ENST00000264692.8:c.1272G>C	ENSP00000264692.5:p.Gly424=
ENST00000403665.6:c.1434G>C	ENSP00000384957.2:p.Gly478=
NM_000128.3:c.1434G>C , LRG_583t1:c.1434G>C	NP_000119.1:p.Gly478=
XM_005262821.2:c.1437G>C	XP_005262878.1:p.Gly479=
XM_005262822.2:c.1437G>C	XP_005262879.1:p.Gly479=
XM_005262823.2:c.1167G>C	XP_005262880.1:p.Gly389=
XM_005262824.1:c.1437G>C	XP_005262881.1:p.Gly479=
XM_006714137.1:c.1389G>C	XP_006714200.1:p.Gly463=
XR_938706.1:n.1842G>C
XR_938707.1:n.1842G>C
XM_005262821.4:c.1437G>C	XP_005262878.1:p.Gly479=
XM_005262822.4:c.1437G>C	XP_005262879.1:p.Gly479=
XM_005262823.4:c.1167G>C	XP_005262880.1:p.Gly389=
XM_006714137.3:c.1389G>C	XP_006714200.1:p.Gly463=
XR_001741172.2:n.1908G>C
NM_000128.4:c.1434G>C MANE Select	NP_000119.1:p.Gly478=