Canonical Allele Identifier: CA388785821

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772754G>C (hg19) ; chr13:g.113118440G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118440G>C , CM000675.2:g.113118440G>C	GRCh38
NC_000013.10:g.113772754G>C , CM000675.1:g.113772754G>C	GRCh37
NC_000013.9:g.112820755G>C	NCBI36
NG_009258.1:g.642G>C , LRG_548:g.642G>C
NG_009262.1:g.17650G>C , LRG_554:g.17650G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.767G>C MANE Select	ENSP00000329546.4:p.Gly256Ala
ENST00000346342.7:c.767G>C	ENSP00000329546.3:p.Gly256Ala
ENST00000375581.3:c.833G>C	ENSP00000364731.3:p.Gly278Ala
ENST00000541084.5:c.581G>C	ENSP00000442051.2:p.Gly194Ala
NM_000131.4:c.833G>C , LRG_554t1:c.833G>C	NP_000122.1:p.Gly278Ala
NM_001267554.1:c.581G>C	NP_001254483.1:p.Gly194Ala
NM_019616.3:c.767G>C , LRG_554t2:c.767G>C	NP_062562.1:p.Gly256Ala
NR_051961.1:n.854G>C
XM_006719963.2:c.626G>C	XP_006720026.1:p.Gly209Ala
XM_011537474.1:c.875G>C	XP_011535776.1:p.Gly292Ala
XM_011537475.1:c.689G>C	XP_011535777.1:p.Gly230Ala
XM_011537476.1:c.527G>C	XP_011535778.1:p.Gly176Ala
XM_011537477.1:c.836G>C	XP_011535779.1:p.Gly279Ala
XM_006719963.3:c.671G>C	XP_006720026.2:p.Gly224Ala
XM_011537474.2:c.920G>C	XP_011535776.2:p.Gly307Ala
XM_011537475.2:c.734G>C	XP_011535777.2:p.Gly245Ala
XM_011537476.2:c.527G>C	XP_011535778.1:p.Gly176Ala
NM_019616.4:c.767G>C MANE Select	NP_062562.1:p.Gly256Ala
NR_051961.2:n.851G>C
NM_001267554.2:c.581G>C	NP_001254483.1:p.Gly194Ala