Canonical Allele Identifier: CA2120141919

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118488A= , CM000675.2:g.113118488A=	GRCh38
NC_000013.10:g.113772802A= , CM000675.1:g.113772802A=	GRCh37
NC_000013.9:g.112820803A=	NCBI36
NG_009258.1:g.690A= , LRG_548:g.690A=
NG_009262.1:g.17698A= , LRG_554:g.17698A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.815A= MANE Select	ENSP00000329546.4:p.Tyr272=
ENST00000346342.7:c.815A=	ENSP00000329546.3:p.Tyr272=
ENST00000375581.3:c.881A=	ENSP00000364731.3:p.Tyr294=
ENST00000541084.5:c.629A=	ENSP00000442051.2:p.Tyr210=
NM_000131.4:c.881A= , LRG_554t1:c.881A=	NP_000122.1:p.Tyr294=
NM_001267554.1:c.629A=	NP_001254483.1:p.Tyr210=
NM_019616.3:c.815A= , LRG_554t2:c.815A=	NP_062562.1:p.Tyr272=
NR_051961.1:n.902A=
XM_006719963.2:c.674A=	XP_006720026.1:p.Tyr225=
XM_011537474.1:c.923A=	XP_011535776.1:p.Tyr308=
XM_011537475.1:c.737A=	XP_011535777.1:p.Tyr246=
XM_011537476.1:c.575A=	XP_011535778.1:p.Tyr192=
XM_011537477.1:c.884A=	XP_011535779.1:p.Tyr295=
XM_006719963.3:c.719A=	XP_006720026.2:p.Tyr240=
XM_011537474.2:c.968A=	XP_011535776.2:p.Tyr323=
XM_011537475.2:c.782A=	XP_011535777.2:p.Tyr261=
XM_011537476.2:c.575A=	XP_011535778.1:p.Tyr192=
NM_019616.4:c.815A= MANE Select	NP_062562.1:p.Tyr272=
NR_051961.2:n.899A=
NM_001267554.2:c.629A=	NP_001254483.1:p.Tyr210=