Canonical Allele Identifier: CA388786487

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773078A>C (hg19) ; chr13:g.113118764A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118764A>C , CM000675.2:g.113118764A>C	GRCh38
NC_000013.10:g.113773078A>C , CM000675.1:g.113773078A>C	GRCh37
NC_000013.9:g.112821079A>C	NCBI36
NG_009258.1:g.966A>C , LRG_548:g.966A>C
NG_009262.1:g.17974A>C , LRG_554:g.17974A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1091A>C MANE Select	ENSP00000329546.4:p.Tyr364Ser
ENST00000346342.7:c.1091A>C	ENSP00000329546.3:p.Tyr364Ser
ENST00000375581.3:c.1157A>C	ENSP00000364731.3:p.Tyr386Ser
ENST00000541084.5:c.905A>C	ENSP00000442051.2:p.Tyr302Ser
NM_000131.4:c.1157A>C , LRG_554t1:c.1157A>C	NP_000122.1:p.Tyr386Ser
NM_001267554.1:c.905A>C	NP_001254483.1:p.Tyr302Ser
NM_019616.3:c.1091A>C , LRG_554t2:c.1091A>C	NP_062562.1:p.Tyr364Ser
NR_051961.1:n.1178A>C
XM_006719963.2:c.950A>C	XP_006720026.1:p.Tyr317Ser
XM_011537474.1:c.1199A>C	XP_011535776.1:p.Tyr400Ser
XM_011537475.1:c.1013A>C	XP_011535777.1:p.Tyr338Ser
XM_011537476.1:c.851A>C	XP_011535778.1:p.Tyr284Ser
XM_011537477.1:c.1160A>C	XP_011535779.1:p.Tyr387Ser
XM_006719963.3:c.995A>C	XP_006720026.2:p.Tyr332Ser
XM_011537474.2:c.1244A>C	XP_011535776.2:p.Tyr415Ser
XM_011537475.2:c.1058A>C	XP_011535777.2:p.Tyr353Ser
XM_011537476.2:c.851A>C	XP_011535778.1:p.Tyr284Ser
NM_019616.4:c.1091A>C MANE Select	NP_062562.1:p.Tyr364Ser
NR_051961.2:n.1175A>C
NM_001267554.2:c.905A>C	NP_001254483.1:p.Tyr302Ser