Canonical Allele Identifier: CA2578522132

Gene: F13A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6182150A>G , CM000668.2:g.6182150A>G	GRCh38
NC_000006.11:g.6182383A>G , CM000668.1:g.6182383A>G	GRCh37
NC_000006.10:g.6127382A>G	NCBI36
NG_008107.1:g.143542T>C , LRG_549:g.143542T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264870.8:c.1306-9T>C MANE Select	ENSP00000264870.3:n.1306-9T>C
ENST00000264870.7:c.1306-9T>C	ENSP00000264870.3:n.1306-9T>C
NM_000129.3:c.1306-9T>C , LRG_549t1:c.1306-9T>C	NP_000120.2:n.1306-9T>C
XM_006715010.2:c.1306-9T>C	XP_006715073.1:n.1306-9T>C
XM_011514342.1:c.1468-9T>C	XP_011512644.1:n.1468-9T>C
NM_000129.4:c.1306-9T>C MANE Select	NP_000120.2:n.1306-9T>C