Canonical Allele Identifier: CA388786732

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773129A>T (hg19) ; chr13:g.113118815A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118815A>T , CM000675.2:g.113118815A>T	GRCh38
NC_000013.10:g.113773129A>T , CM000675.1:g.113773129A>T	GRCh37
NC_000013.9:g.112821130A>T	NCBI36
NG_009258.1:g.1017A>T , LRG_548:g.1017A>T
NG_009262.1:g.18025A>T , LRG_554:g.18025A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1142A>T MANE Select	ENSP00000329546.4:p.Asp381Val
ENST00000346342.7:c.1142A>T	ENSP00000329546.3:p.Asp381Val
ENST00000375581.3:c.1208A>T	ENSP00000364731.3:p.Asp403Val
ENST00000541084.5:c.956A>T	ENSP00000442051.2:p.Asp319Val
NM_000131.4:c.1208A>T , LRG_554t1:c.1208A>T	NP_000122.1:p.Asp403Val
NM_001267554.1:c.956A>T	NP_001254483.1:p.Asp319Val
NM_019616.3:c.1142A>T , LRG_554t2:c.1142A>T	NP_062562.1:p.Asp381Val
NR_051961.1:n.1229A>T
XM_006719963.2:c.1001A>T	XP_006720026.1:p.Asp334Val
XM_011537474.1:c.1250A>T	XP_011535776.1:p.Asp417Val
XM_011537475.1:c.1064A>T	XP_011535777.1:p.Asp355Val
XM_011537476.1:c.902A>T	XP_011535778.1:p.Asp301Val
XM_011537477.1:c.1211A>T	XP_011535779.1:p.Asp404Val
XM_006719963.3:c.1046A>T	XP_006720026.2:p.Asp349Val
XM_011537474.2:c.1295A>T	XP_011535776.2:p.Asp432Val
XM_011537475.2:c.1109A>T	XP_011535777.2:p.Asp370Val
XM_011537476.2:c.902A>T	XP_011535778.1:p.Asp301Val
NM_019616.4:c.1142A>T MANE Select	NP_062562.1:p.Asp381Val
NR_051961.2:n.1226A>T
NM_001267554.2:c.956A>T	NP_001254483.1:p.Asp319Val