Canonical Allele Identifier: CA565359588

Gene: F13A1

Linked Data

• dbSNP Id: rs1442033828
• gnomAD v2: 6-6182380-AACAGGAGAGGAG-A
• gnomAD v4: 6-6182147-AACAGGAGAGGAG-A
• MyVariant Identifiers: chr6:g.6182381_6182392del (hg19) ; chr6:g.6182148_6182159del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6182149_6182160del , CM000668.2:g.6182149_6182160del	GRCh38
NC_000006.11:g.6182382_6182393del , CM000668.1:g.6182382_6182393del	GRCh37
NC_000006.10:g.6127381_6127392del	NCBI36
NG_008107.1:g.143533_143544del , LRG_549:g.143533_143544del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264870.8:c.1306-18_1306-7del MANE Select	ENSP00000264870.3:n.1306-18_1306-7del
ENST00000264870.7:c.1306-18_1306-7del	ENSP00000264870.3:n.1306-18_1306-7del
NM_000129.3:c.1306-18_1306-7del , LRG_549t1:c.1306-18_1306-7del	NP_000120.2:n.1306-18_1306-7del
XM_006715010.2:c.1306-18_1306-7del	XP_006715073.1:n.1306-18_1306-7del
XM_011514342.1:c.1468-18_1468-7del	XP_011512644.1:n.1468-18_1468-7del
NM_000129.4:c.1306-18_1306-7del MANE Select	NP_000120.2:n.1306-18_1306-7del