Canonical Allele Identifier: CA1608030297

Gene: F13A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6318517_6318518delinsAG , CM000668.2:g.6318517_6318518delinsAG	GRCh38
NC_000006.11:g.6318750_6318751delinsAG , CM000668.1:g.6318750_6318751delinsAG	GRCh37
NC_000006.10:g.6263749_6263750delinsAG	NCBI36
NG_008107.1:g.7174_7175delinsCT , LRG_549:g.7174_7175delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264870.8:c.130+17_130+18delinsCT MANE Select	ENSP00000264870.3:n.130+17_130+18delinsCT
ENST00000264870.7:c.130+17_130+18delinsCT	ENSP00000264870.3:n.130+17_130+18delinsCT
ENST00000414279.5:c.130+17_130+18delinsCT	ENSP00000413334.1:n.130+17_130+18delinsCT
ENST00000431222.6:c.292+17_292+18delinsCT	ENSP00000416295.2:n.292+17_292+18delinsCT
ENST00000451619.1:c.204+17_204+18delinsCT
NM_000129.3:c.130+17_130+18delinsCT , LRG_549t1:c.130+17_130+18delinsCT	NP_000120.2:n.130+17_130+18delinsCT
XM_006715010.2:c.130+17_130+18delinsCT	XP_006715073.1:n.130+17_130+18delinsCT
XM_011514342.1:c.292+17_292+18delinsCT	XP_011512644.1:n.292+17_292+18delinsCT
NM_000129.4:c.130+17_130+18delinsCT MANE Select	NP_000120.2:n.130+17_130+18delinsCT