Canonical Allele Identifier: CA388792551

Gene: F10

Linked Data

• MyVariant Identifiers: chr13:g.113803370A>T (hg19) ; chr13:g.113149056A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149056A>T , CM000675.2:g.113149056A>T	GRCh38
NC_000013.10:g.113803370A>T , CM000675.1:g.113803370A>T	GRCh37
NC_000013.9:g.112851371A>T	NCBI36
NG_009258.1:g.31258A>T , LRG_548:g.31258A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000375559.8:c.1006A>T MANE Select	ENSP00000364709.3:p.Met336Leu
ENST00000375551.7:c.996A>T	ENSP00000364701.3:p.Ala332=
ENST00000375559.7:c.1006A>T	ENSP00000364709.3:p.Met336Leu
ENST00000409306.5:c.1002A>T	ENSP00000387092.1:p.Ala334=
NM_000504.3:c.1006A>T , LRG_548t1:c.1006A>T	NP_000495.1:p.Met336Leu
NM_001312674.1:c.874A>T	NP_001299603.1:p.Met292Leu
NM_001312675.1:c.996A>T	NP_001299604.1:p.Ala332=
NM_000504.4:c.1006A>T MANE Select	NP_000495.1:p.Met336Leu
NM_001312674.2:c.874A>T	NP_001299603.1:p.Met292Leu
NM_001312675.2:c.996A>T	NP_001299604.1:p.Ala332=