Canonical Allele Identifier: CA442639111
Gene: F11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.187205376A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186284222A>C , CM000666.2:g.186284222A>C GRCh38
NC_000004.11:g.187205376A>C , CM000666.1:g.187205376A>C GRCh37
NC_000004.10:g.187442370A>C NCBI36
NG_008051.1:g.23259A>C , LRG_583:g.23259A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.1266A>C MANE Select ENSP00000384957.2:p.Gly422=
ENST00000264692.8:c.1104A>C ENSP00000264692.5:p.Gly368=
ENST00000403665.6:c.1266A>C ENSP00000384957.2:p.Gly422=
NM_000128.3:c.1266A>C , LRG_583t1:c.1266A>C NP_000119.1:p.Gly422=
XM_005262821.2:c.1269A>C XP_005262878.1:p.Gly423=
XM_005262822.2:c.1269A>C XP_005262879.1:p.Gly423=
XM_005262823.2:c.999A>C XP_005262880.1:p.Gly333=
XM_005262824.1:c.1269A>C XP_005262881.1:p.Gly423=
XM_006714137.1:c.1221A>C XP_006714200.1:p.Gly407=
XR_938706.1:n.1674A>C
XR_938707.1:n.1674A>C
XM_005262821.4:c.1269A>C XP_005262878.1:p.Gly423=
XM_005262822.4:c.1269A>C XP_005262879.1:p.Gly423=
XM_005262823.4:c.999A>C XP_005262880.1:p.Gly333=
XM_006714137.3:c.1221A>C XP_006714200.1:p.Gly407=
XR_001741172.2:n.1740A>C
NM_000128.4:c.1266A>C MANE Select NP_000119.1:p.Gly422=