Canonical Allele Identifier: CA388791201

Gene: F10

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113147461G>C , CM000675.2:g.113147461G>C	GRCh38
NC_000013.10:g.113801775G>C , CM000675.1:g.113801775G>C	GRCh37
NC_000013.9:g.112849776G>C	NCBI36
NG_009258.1:g.29663G>C , LRG_548:g.29663G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000504.4:c.830G>C MANE Select	NP_000495.1:p.Cys277Ser
ENST00000375559.8:c.830G>C MANE Select	ENSP00000364709.3:p.Cys277Ser
NM_000504.3:c.830G>C , LRG_548t1:c.830G>C	NP_000495.1:p.Cys277Ser
NM_001312674.1:c.698G>C	NP_001299603.1:p.Cys233Ser
NM_001312674.2:c.698G>C	NP_001299603.1:p.Cys233Ser
NM_001312675.1:c.830G>C	NP_001299604.1:p.Cys277Ser
NM_001312675.2:c.830G>C	NP_001299604.1:p.Cys277Ser
ENST00000375551.7:c.830G>C	ENSP00000364701.3:p.Cys277Ser
ENST00000375559.7:c.830G>C	ENSP00000364709.3:p.Cys277Ser
ENST00000409306.5:c.830G>C	ENSP00000387092.1:p.Cys277Ser
ENST00000410083.6:c.*789G>C	ENSP00000386320.2:n.*789G>C