Canonical Allele Identifier: CA362655830

Gene: F13A1

Linked Data

• MyVariant Identifiers: chr6:g.6145859G>T (hg19) ; chr6:g.6145626G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6145626G>T , CM000668.2:g.6145626G>T	GRCh38
NC_000006.11:g.6145859G>T , CM000668.1:g.6145859G>T	GRCh37
NC_000006.10:g.6090858G>T	NCBI36
NG_008107.1:g.180066C>A , LRG_549:g.180066C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264870.8:c.2192C>A MANE Select	ENSP00000264870.3:p.Ser731Tyr
ENST00000264870.7:c.2192C>A	ENSP00000264870.3:p.Ser731Tyr
NM_000129.3:c.2192C>A , LRG_549t1:c.2192C>A	NP_000120.2:p.Ser731Tyr
XM_006715010.2:c.2192C>A	XP_006715073.1:p.Ser731Tyr
XM_011514342.1:c.2354C>A	XP_011512644.1:p.Ser785Tyr
NM_000129.4:c.2192C>A MANE Select	NP_000120.2:p.Ser731Tyr