Canonical Allele Identifier: CA448640526

Gene: F13A1

Linked Data

• MyVariant Identifiers: chr6:g.6182321C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.6182088C>G , CM000668.2:g.6182088C>G	GRCh38
NC_000006.11:g.6182321C>G , CM000668.1:g.6182321C>G	GRCh37
NC_000006.10:g.6127320C>G	NCBI36
NG_008107.1:g.143604G>C , LRG_549:g.143604G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264870.8:c.1359G>C MANE Select	ENSP00000264870.3:p.Val453=
ENST00000264870.7:c.1359G>C	ENSP00000264870.3:p.Val453=
NM_000129.3:c.1359G>C , LRG_549t1:c.1359G>C	NP_000120.2:p.Val453=
XM_006715010.2:c.1359G>C	XP_006715073.1:p.Val453=
XM_011514342.1:c.1521G>C	XP_011512644.1:p.Val507=
NM_000129.4:c.1359G>C MANE Select	NP_000120.2:p.Val453=