Canonical Allele Identifier: CA388786825

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773150C>G (hg19) ; chr13:g.113118836C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118836C>G , CM000675.2:g.113118836C>G	GRCh38
NC_000013.10:g.113773150C>G , CM000675.1:g.113773150C>G	GRCh37
NC_000013.9:g.112821151C>G	NCBI36
NG_009258.1:g.1038C>G , LRG_548:g.1038C>G
NG_009262.1:g.18046C>G , LRG_554:g.18046C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1163C>G MANE Select	ENSP00000329546.4:p.Thr388Ser
ENST00000346342.7:c.1163C>G	ENSP00000329546.3:p.Thr388Ser
ENST00000375581.3:c.1229C>G	ENSP00000364731.3:p.Thr410Ser
ENST00000541084.5:c.977C>G	ENSP00000442051.2:p.Thr326Ser
NM_000131.4:c.1229C>G , LRG_554t1:c.1229C>G	NP_000122.1:p.Thr410Ser
NM_001267554.1:c.977C>G	NP_001254483.1:p.Thr326Ser
NM_019616.3:c.1163C>G , LRG_554t2:c.1163C>G	NP_062562.1:p.Thr388Ser
NR_051961.1:n.1250C>G
XM_006719963.2:c.1022C>G	XP_006720026.1:p.Thr341Ser
XM_011537474.1:c.1271C>G	XP_011535776.1:p.Thr424Ser
XM_011537475.1:c.1085C>G	XP_011535777.1:p.Thr362Ser
XM_011537476.1:c.923C>G	XP_011535778.1:p.Thr308Ser
XM_011537477.1:c.1232C>G	XP_011535779.1:p.Thr411Ser
XM_006719963.3:c.1067C>G	XP_006720026.2:p.Thr356Ser
XM_011537474.2:c.1316C>G	XP_011535776.2:p.Thr439Ser
XM_011537475.2:c.1130C>G	XP_011535777.2:p.Thr377Ser
XM_011537476.2:c.923C>G	XP_011535778.1:p.Thr308Ser
NM_019616.4:c.1163C>G MANE Select	NP_062562.1:p.Thr388Ser
NR_051961.2:n.1247C>G
NM_001267554.2:c.977C>G	NP_001254483.1:p.Thr326Ser