Canonical Allele Identifier: CA388786159

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772928T>C (hg19) ; chr13:g.113118614T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118614T>C , CM000675.2:g.113118614T>C	GRCh38
NC_000013.10:g.113772928T>C , CM000675.1:g.113772928T>C	GRCh37
NC_000013.9:g.112820929T>C	NCBI36
NG_009258.1:g.816T>C , LRG_548:g.816T>C
NG_009262.1:g.17824T>C , LRG_554:g.17824T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.941T>C MANE Select	ENSP00000329546.4:p.Val314Ala
ENST00000346342.7:c.941T>C	ENSP00000329546.3:p.Val314Ala
ENST00000375581.3:c.1007T>C	ENSP00000364731.3:p.Val336Ala
ENST00000541084.5:c.755T>C	ENSP00000442051.2:p.Val252Ala
NM_000131.4:c.1007T>C , LRG_554t1:c.1007T>C	NP_000122.1:p.Val336Ala
NM_001267554.1:c.755T>C	NP_001254483.1:p.Val252Ala
NM_019616.3:c.941T>C , LRG_554t2:c.941T>C	NP_062562.1:p.Val314Ala
NR_051961.1:n.1028T>C
XM_006719963.2:c.800T>C	XP_006720026.1:p.Val267Ala
XM_011537474.1:c.1049T>C	XP_011535776.1:p.Val350Ala
XM_011537475.1:c.863T>C	XP_011535777.1:p.Val288Ala
XM_011537476.1:c.701T>C	XP_011535778.1:p.Val234Ala
XM_011537477.1:c.1010T>C	XP_011535779.1:p.Val337Ala
XM_006719963.3:c.845T>C	XP_006720026.2:p.Val282Ala
XM_011537474.2:c.1094T>C	XP_011535776.2:p.Val365Ala
XM_011537475.2:c.908T>C	XP_011535777.2:p.Val303Ala
XM_011537476.2:c.701T>C	XP_011535778.1:p.Val234Ala
NM_019616.4:c.941T>C MANE Select	NP_062562.1:p.Val314Ala
NR_051961.2:n.1025T>C
NM_001267554.2:c.755T>C	NP_001254483.1:p.Val252Ala