Canonical Allele Identifier: CA388786796

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773144A>C (hg19) ; chr13:g.113118830A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118830A>C , CM000675.2:g.113118830A>C	GRCh38
NC_000013.10:g.113773144A>C , CM000675.1:g.113773144A>C	GRCh37
NC_000013.9:g.112821145A>C	NCBI36
NG_009258.1:g.1032A>C , LRG_548:g.1032A>C
NG_009262.1:g.18040A>C , LRG_554:g.18040A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1157A>C MANE Select	ENSP00000329546.4:p.His386Pro
ENST00000346342.7:c.1157A>C	ENSP00000329546.3:p.His386Pro
ENST00000375581.3:c.1223A>C	ENSP00000364731.3:p.His408Pro
ENST00000541084.5:c.971A>C	ENSP00000442051.2:p.His324Pro
NM_000131.4:c.1223A>C , LRG_554t1:c.1223A>C	NP_000122.1:p.His408Pro
NM_001267554.1:c.971A>C	NP_001254483.1:p.His324Pro
NM_019616.3:c.1157A>C , LRG_554t2:c.1157A>C	NP_062562.1:p.His386Pro
NR_051961.1:n.1244A>C
XM_006719963.2:c.1016A>C	XP_006720026.1:p.His339Pro
XM_011537474.1:c.1265A>C	XP_011535776.1:p.His422Pro
XM_011537475.1:c.1079A>C	XP_011535777.1:p.His360Pro
XM_011537476.1:c.917A>C	XP_011535778.1:p.His306Pro
XM_011537477.1:c.1226A>C	XP_011535779.1:p.His409Pro
XM_006719963.3:c.1061A>C	XP_006720026.2:p.His354Pro
XM_011537474.2:c.1310A>C	XP_011535776.2:p.His437Pro
XM_011537475.2:c.1124A>C	XP_011535777.2:p.His375Pro
XM_011537476.2:c.917A>C	XP_011535778.1:p.His306Pro
NM_019616.4:c.1157A>C MANE Select	NP_062562.1:p.His386Pro
NR_051961.2:n.1241A>C
NM_001267554.2:c.971A>C	NP_001254483.1:p.His324Pro