Canonical Allele Identifier: CA388787180

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773284C>A (hg19) ; chr13:g.113118970C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118970C>A , CM000675.2:g.113118970C>A	GRCh38
NC_000013.10:g.113773284C>A , CM000675.1:g.113773284C>A	GRCh37
NC_000013.9:g.112821285C>A	NCBI36
NG_009258.1:g.1172C>A , LRG_548:g.1172C>A
NG_009262.1:g.18180C>A , LRG_554:g.18180C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1297C>A MANE Select	ENSP00000329546.4:p.Pro433Thr
ENST00000346342.7:c.1297C>A	ENSP00000329546.3:p.Pro433Thr
ENST00000375581.3:c.1363C>A	ENSP00000364731.3:p.Pro455Thr
ENST00000541084.5:c.1111C>A	ENSP00000442051.2:p.Pro371Thr
NM_000131.4:c.1363C>A , LRG_554t1:c.1363C>A	NP_000122.1:p.Pro455Thr
NM_001267554.1:c.1111C>A	NP_001254483.1:p.Pro371Thr
NM_019616.3:c.1297C>A , LRG_554t2:c.1297C>A	NP_062562.1:p.Pro433Thr
NR_051961.1:n.1384C>A
XM_006719963.2:c.1156C>A	XP_006720026.1:p.Pro386Thr
XM_011537474.1:c.1405C>A	XP_011535776.1:p.Pro469Thr
XM_011537475.1:c.1219C>A	XP_011535777.1:p.Pro407Thr
XM_011537476.1:c.1057C>A	XP_011535778.1:p.Pro353Thr
XM_011537477.1:c.1366C>A	XP_011535779.1:p.Pro456Thr
XM_006719963.3:c.1201C>A	XP_006720026.2:p.Pro401Thr
XM_011537474.2:c.1450C>A	XP_011535776.2:p.Pro484Thr
XM_011537475.2:c.1264C>A	XP_011535777.2:p.Pro422Thr
XM_011537476.2:c.1057C>A	XP_011535778.1:p.Pro353Thr
NM_019616.4:c.1297C>A MANE Select	NP_062562.1:p.Pro433Thr
NR_051961.2:n.1381C>A
NM_001267554.2:c.1111C>A	NP_001254483.1:p.Pro371Thr