Canonical Allele Identifier: CA485423940

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772923C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118609C>T , CM000675.2:g.113118609C>T	GRCh38
NC_000013.10:g.113772923C>T , CM000675.1:g.113772923C>T	GRCh37
NC_000013.9:g.112820924C>T	NCBI36
NG_009258.1:g.811C>T , LRG_548:g.811C>T
NG_009262.1:g.17819C>T , LRG_554:g.17819C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.936C>T MANE Select	ENSP00000329546.4:p.Ala312=
ENST00000346342.7:c.936C>T	ENSP00000329546.3:p.Ala312=
ENST00000375581.3:c.1002C>T	ENSP00000364731.3:p.Ala334=
ENST00000541084.5:c.750C>T	ENSP00000442051.2:p.Ala250=
NM_000131.4:c.1002C>T , LRG_554t1:c.1002C>T	NP_000122.1:p.Ala334=
NM_001267554.1:c.750C>T	NP_001254483.1:p.Ala250=
NM_019616.3:c.936C>T , LRG_554t2:c.936C>T	NP_062562.1:p.Ala312=
NR_051961.1:n.1023C>T
XM_006719963.2:c.795C>T	XP_006720026.1:p.Ala265=
XM_011537474.1:c.1044C>T	XP_011535776.1:p.Ala348=
XM_011537475.1:c.858C>T	XP_011535777.1:p.Ala286=
XM_011537476.1:c.696C>T	XP_011535778.1:p.Ala232=
XM_011537477.1:c.1005C>T	XP_011535779.1:p.Ala335=
XM_006719963.3:c.840C>T	XP_006720026.2:p.Ala280=
XM_011537474.2:c.1089C>T	XP_011535776.2:p.Ala363=
XM_011537475.2:c.903C>T	XP_011535777.2:p.Ala301=
XM_011537476.2:c.696C>T	XP_011535778.1:p.Ala232=
NM_019616.4:c.936C>T MANE Select	NP_062562.1:p.Ala312=
NR_051961.2:n.1020C>T
NM_001267554.2:c.750C>T	NP_001254483.1:p.Ala250=