Canonical Allele Identifier: CA2120142713

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118807C= , CM000675.2:g.113118807C=	GRCh38
NC_000013.10:g.113773121C= , CM000675.1:g.113773121C=	GRCh37
NC_000013.9:g.112821122C=	NCBI36
NG_009258.1:g.1009C= , LRG_548:g.1009C=
NG_009262.1:g.18017C= , LRG_554:g.18017C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1134C= MANE Select	ENSP00000329546.4:p.Cys378=
ENST00000346342.7:c.1134C=	ENSP00000329546.3:p.Cys378=
ENST00000375581.3:c.1200C=	ENSP00000364731.3:p.Cys400=
ENST00000541084.5:c.948C=	ENSP00000442051.2:p.Cys316=
NM_000131.4:c.1200C= , LRG_554t1:c.1200C=	NP_000122.1:p.Cys400=
NM_001267554.1:c.948C=	NP_001254483.1:p.Cys316=
NM_019616.3:c.1134C= , LRG_554t2:c.1134C=	NP_062562.1:p.Cys378=
NR_051961.1:n.1221C=
XM_006719963.2:c.993C=	XP_006720026.1:p.Cys331=
XM_011537474.1:c.1242C=	XP_011535776.1:p.Cys414=
XM_011537475.1:c.1056C=	XP_011535777.1:p.Cys352=
XM_011537476.1:c.894C=	XP_011535778.1:p.Cys298=
XM_011537477.1:c.1203C=	XP_011535779.1:p.Cys401=
XM_006719963.3:c.1038C=	XP_006720026.2:p.Cys346=
XM_011537474.2:c.1287C=	XP_011535776.2:p.Cys429=
XM_011537475.2:c.1101C=	XP_011535777.2:p.Cys367=
XM_011537476.2:c.894C=	XP_011535778.1:p.Cys298=
NM_019616.4:c.1134C= MANE Select	NP_062562.1:p.Cys378=
NR_051961.2:n.1218C=
NM_001267554.2:c.948C=	NP_001254483.1:p.Cys316=