Canonical Allele Identifier: CA13803763

Gene: F10

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113141357T>C , CM000675.2:g.113141357T>C	GRCh38
NC_000013.10:g.113795671T>C , CM000675.1:g.113795671T>C	GRCh37
NC_000013.9:g.112843672T>C	NCBI36
NG_009258.1:g.23559T>C , LRG_548:g.23559T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.502+307T>C MANE Select	ENSP00000364709.3:n.502+307T>C
ENST00000375551.7:c.502+307T>C	ENSP00000364701.3:n.502+307T>C
ENST00000375559.7:c.502+307T>C	ENSP00000364709.3:n.502+307T>C
ENST00000409306.5:c.502+307T>C	ENSP00000387092.1:n.502+307T>C
ENST00000410083.6:c.*461+307T>C	ENSP00000386320.2:n.*461+307T>C
ENST00000477269.5:n.539+307T>C
ENST00000498455.1:n.531+307T>C
NM_000504.3:c.502+307T>C , LRG_548t1:c.502+307T>C	NP_000495.1:n.502+307T>C
NM_001312674.1:c.370+1887T>C	NP_001299603.1:n.370+1887T>C
NM_001312675.1:c.502+307T>C	NP_001299604.1:n.502+307T>C
NM_000504.4:c.502+307T>C MANE Select	NP_000495.1:n.502+307T>C
NM_001312674.2:c.370+1887T>C	NP_001299603.1:n.370+1887T>C
NM_001312675.2:c.502+307T>C	NP_001299604.1:n.502+307T>C