Canonical Allele Identifier: CA388793647

Gene: F10

Linked Data

• MyVariant Identifiers: chr13:g.113803569T>C (hg19) ; chr13:g.113149255T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149255T>C , CM000675.2:g.113149255T>C	GRCh38
NC_000013.10:g.113803569T>C , CM000675.1:g.113803569T>C	GRCh37
NC_000013.9:g.112851570T>C	NCBI36
NG_009258.1:g.31457T>C , LRG_548:g.31457T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.1205T>C MANE Select	ENSP00000364709.3:p.Met402Thr
ENST00000375551.7:c.*196T>C	ENSP00000364701.3:n.*196T>C
ENST00000375559.7:c.1205T>C	ENSP00000364709.3:p.Met402Thr
ENST00000409306.5:c.*196T>C	ENSP00000387092.1:n.*196T>C
NM_000504.3:c.1205T>C , LRG_548t1:c.1205T>C	NP_000495.1:p.Met402Thr
NM_001312674.1:c.1073T>C	NP_001299603.1:p.Met358Thr
NM_001312675.1:c.*196T>C	NP_001299604.1:n.*196T>C
NM_000504.4:c.1205T>C MANE Select	NP_000495.1:p.Met402Thr
NM_001312674.2:c.1073T>C	NP_001299603.1:p.Met358Thr
NM_001312675.2:c.*196T>C	NP_001299604.1:n.*196T>C