Canonical Allele Identifier: CA134400208

Gene: F13A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6305244C>A , CM000668.2:g.6305244C>A	GRCh38
NC_000006.11:g.6305477C>A , CM000668.1:g.6305477C>A	GRCh37
NC_000006.10:g.6250476C>A	NCBI36
NG_008107.1:g.20448G>T , LRG_549:g.20448G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264870.8:c.319+107G>T MANE Select	ENSP00000264870.3:n.319+107G>T
ENST00000264870.7:c.319+107G>T	ENSP00000264870.3:n.319+107G>T
ENST00000414279.5:c.319+107G>T	ENSP00000413334.1:n.319+107G>T
ENST00000431222.6:c.481+107G>T	ENSP00000416295.2:n.481+107G>T
ENST00000451619.1:c.500G>T
ENST00000479211.1:n.304+107G>T
NM_000129.3:c.319+107G>T , LRG_549t1:c.319+107G>T	NP_000120.2:n.319+107G>T
XM_006715010.2:c.319+107G>T	XP_006715073.1:n.319+107G>T
XM_011514342.1:c.481+107G>T	XP_011512644.1:n.481+107G>T
NM_000129.4:c.319+107G>T MANE Select	NP_000120.2:n.319+107G>T