Canonical Allele Identifier: CA362740412

Gene: F13A1

Linked Data

• MyVariant Identifiers: chr6:g.6248622A>C (hg19) ; chr6:g.6248389A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6248389A>C , CM000668.2:g.6248389A>C	GRCh38
NC_000006.11:g.6248622A>C , CM000668.1:g.6248622A>C	GRCh37
NC_000006.10:g.6193621A>C	NCBI36
NG_008107.1:g.77303T>G , LRG_549:g.77303T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264870.8:c.721T>G MANE Select	ENSP00000264870.3:p.Tyr241Asp
ENST00000264870.7:c.721T>G	ENSP00000264870.3:p.Tyr241Asp
NM_000129.3:c.721T>G , LRG_549t1:c.721T>G	NP_000120.2:p.Tyr241Asp
XM_006715010.2:c.721T>G	XP_006715073.1:p.Tyr241Asp
XM_011514342.1:c.883T>G	XP_011512644.1:p.Tyr295Asp
NM_000129.4:c.721T>G MANE Select	NP_000120.2:p.Tyr241Asp