Canonical Allele Identifier: CA358939847

Gene: F11

Linked Data

• dbSNP Id: rs1226426769
• gnomAD v2: 4-187201726-T-C
• gnomAD v4: 4-186280572-T-C
• MyVariant Identifiers: chr4:g.187201726T>C (hg19) ; chr4:g.186280572T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186280572T>C , CM000666.2:g.186280572T>C	GRCh38
NC_000004.11:g.187201726T>C , CM000666.1:g.187201726T>C	GRCh37
NC_000004.10:g.187438720T>C	NCBI36
NG_008051.1:g.19609T>C , LRG_583:g.19609T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1127T>C MANE Select	ENSP00000384957.2:p.Met376Thr
ENST00000264692.8:c.965T>C	ENSP00000264692.5:p.Met322Thr
ENST00000403665.6:c.1127T>C	ENSP00000384957.2:p.Met376Thr
ENST00000452239.1:c.574T>C
NM_000128.3:c.1127T>C , LRG_583t1:c.1127T>C	NP_000119.1:p.Met376Thr
XM_005262821.2:c.1130T>C	XP_005262878.1:p.Met377Thr
XM_005262822.2:c.1130T>C	XP_005262879.1:p.Met377Thr
XM_005262823.2:c.860T>C	XP_005262880.1:p.Met287Thr
XM_005262824.1:c.1130T>C	XP_005262881.1:p.Met377Thr
XM_006714137.1:c.1082T>C	XP_006714200.1:p.Met361Thr
XR_938706.1:n.1482T>C
XR_938707.1:n.1482T>C
XM_005262821.4:c.1130T>C	XP_005262878.1:p.Met377Thr
XM_005262822.4:c.1130T>C	XP_005262879.1:p.Met377Thr
XM_005262823.4:c.860T>C	XP_005262880.1:p.Met287Thr
XM_006714137.3:c.1082T>C	XP_006714200.1:p.Met361Thr
XM_017007884.2:c.1130T>C	XP_016863373.1:p.Met377Thr
XM_017007885.2:c.1130T>C	XP_016863374.1:p.Met377Thr
XM_017007886.2:c.1127T>C	XP_016863375.1:p.Met376Thr
XR_001741172.2:n.1548T>C
NM_000128.4:c.1127T>C MANE Select	NP_000119.1:p.Met376Thr