Canonical Allele Identifier: CA388786268

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772985T>A (hg19) ; chr13:g.113118671T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118671T>A , CM000675.2:g.113118671T>A	GRCh38
NC_000013.10:g.113772985T>A , CM000675.1:g.113772985T>A	GRCh37
NC_000013.9:g.112820986T>A	NCBI36
NG_009258.1:g.873T>A , LRG_548:g.873T>A
NG_009262.1:g.17881T>A , LRG_554:g.17881T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.998T>A MANE Select	ENSP00000329546.4:p.Leu333Gln
ENST00000346342.7:c.998T>A	ENSP00000329546.3:p.Leu333Gln
ENST00000375581.3:c.1064T>A	ENSP00000364731.3:p.Leu355Gln
ENST00000541084.5:c.812T>A	ENSP00000442051.2:p.Leu271Gln
NM_000131.4:c.1064T>A , LRG_554t1:c.1064T>A	NP_000122.1:p.Leu355Gln
NM_001267554.1:c.812T>A	NP_001254483.1:p.Leu271Gln
NM_019616.3:c.998T>A , LRG_554t2:c.998T>A	NP_062562.1:p.Leu333Gln
NR_051961.1:n.1085T>A
XM_006719963.2:c.857T>A	XP_006720026.1:p.Leu286Gln
XM_011537474.1:c.1106T>A	XP_011535776.1:p.Leu369Gln
XM_011537475.1:c.920T>A	XP_011535777.1:p.Leu307Gln
XM_011537476.1:c.758T>A	XP_011535778.1:p.Leu253Gln
XM_011537477.1:c.1067T>A	XP_011535779.1:p.Leu356Gln
XM_006719963.3:c.902T>A	XP_006720026.2:p.Leu301Gln
XM_011537474.2:c.1151T>A	XP_011535776.2:p.Leu384Gln
XM_011537475.2:c.965T>A	XP_011535777.2:p.Leu322Gln
XM_011537476.2:c.758T>A	XP_011535778.1:p.Leu253Gln
NM_019616.4:c.998T>A MANE Select	NP_062562.1:p.Leu333Gln
NR_051961.2:n.1082T>A
NM_001267554.2:c.812T>A	NP_001254483.1:p.Leu271Gln