Canonical Allele Identifier: CA388786180

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772940T>A (hg19) ; chr13:g.113118626T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118626T>A , CM000675.2:g.113118626T>A	GRCh38
NC_000013.10:g.113772940T>A , CM000675.1:g.113772940T>A	GRCh37
NC_000013.9:g.112820941T>A	NCBI36
NG_009258.1:g.828T>A , LRG_548:g.828T>A
NG_009262.1:g.17836T>A , LRG_554:g.17836T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.953T>A MANE Select	ENSP00000329546.4:p.Leu318Ter
ENST00000346342.7:c.953T>A	ENSP00000329546.3:p.Leu318Ter
ENST00000375581.3:c.1019T>A	ENSP00000364731.3:p.Leu340Ter
ENST00000541084.5:c.767T>A	ENSP00000442051.2:p.Leu256Ter
NM_000131.4:c.1019T>A , LRG_554t1:c.1019T>A	NP_000122.1:p.Leu340Ter
NM_001267554.1:c.767T>A	NP_001254483.1:p.Leu256Ter
NM_019616.3:c.953T>A , LRG_554t2:c.953T>A	NP_062562.1:p.Leu318Ter
NR_051961.1:n.1040T>A
XM_006719963.2:c.812T>A	XP_006720026.1:p.Leu271Ter
XM_011537474.1:c.1061T>A	XP_011535776.1:p.Leu354Ter
XM_011537475.1:c.875T>A	XP_011535777.1:p.Leu292Ter
XM_011537476.1:c.713T>A	XP_011535778.1:p.Leu238Ter
XM_011537477.1:c.1022T>A	XP_011535779.1:p.Leu341Ter
XM_006719963.3:c.857T>A	XP_006720026.2:p.Leu286Ter
XM_011537474.2:c.1106T>A	XP_011535776.2:p.Leu369Ter
XM_011537475.2:c.920T>A	XP_011535777.2:p.Leu307Ter
XM_011537476.2:c.713T>A	XP_011535778.1:p.Leu238Ter
NM_019616.4:c.953T>A MANE Select	NP_062562.1:p.Leu318Ter
NR_051961.2:n.1037T>A
NM_001267554.2:c.767T>A	NP_001254483.1:p.Leu256Ter