Canonical Allele Identifier: CA388786525

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773085C>A (hg19) ; chr13:g.113118771C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118771C>A , CM000675.2:g.113118771C>A	GRCh38
NC_000013.10:g.113773085C>A , CM000675.1:g.113773085C>A	GRCh37
NC_000013.9:g.112821086C>A	NCBI36
NG_009258.1:g.973C>A , LRG_548:g.973C>A
NG_009262.1:g.17981C>A , LRG_554:g.17981C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1098C>A MANE Select	ENSP00000329546.4:p.Phe366Leu
ENST00000346342.7:c.1098C>A	ENSP00000329546.3:p.Phe366Leu
ENST00000375581.3:c.1164C>A	ENSP00000364731.3:p.Phe388Leu
ENST00000541084.5:c.912C>A	ENSP00000442051.2:p.Phe304Leu
NM_000131.4:c.1164C>A , LRG_554t1:c.1164C>A	NP_000122.1:p.Phe388Leu
NM_001267554.1:c.912C>A	NP_001254483.1:p.Phe304Leu
NM_019616.3:c.1098C>A , LRG_554t2:c.1098C>A	NP_062562.1:p.Phe366Leu
NR_051961.1:n.1185C>A
XM_006719963.2:c.957C>A	XP_006720026.1:p.Phe319Leu
XM_011537474.1:c.1206C>A	XP_011535776.1:p.Phe402Leu
XM_011537475.1:c.1020C>A	XP_011535777.1:p.Phe340Leu
XM_011537476.1:c.858C>A	XP_011535778.1:p.Phe286Leu
XM_011537477.1:c.1167C>A	XP_011535779.1:p.Phe389Leu
XM_006719963.3:c.1002C>A	XP_006720026.2:p.Phe334Leu
XM_011537474.2:c.1251C>A	XP_011535776.2:p.Phe417Leu
XM_011537475.2:c.1065C>A	XP_011535777.2:p.Phe355Leu
XM_011537476.2:c.858C>A	XP_011535778.1:p.Phe286Leu
NM_019616.4:c.1098C>A MANE Select	NP_062562.1:p.Phe366Leu
NR_051961.2:n.1182C>A
NM_001267554.2:c.912C>A	NP_001254483.1:p.Phe304Leu