Canonical Allele Identifier: CA1607973347
Gene: F13A1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6181923G= , CM000668.2:g.6181923G= GRCh38
NC_000006.11:g.6182156G= , CM000668.1:g.6182156G= GRCh37
NC_000006.10:g.6127155G= NCBI36
NG_008107.1:g.143769C= , LRG_549:g.143769C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264870.8:c.1459+65C= MANE Select ENSP00000264870.3:n.1459+65C=
ENST00000264870.7:c.1459+65C= ENSP00000264870.3:n.1459+65C=
NM_000129.3:c.1459+65C= , LRG_549t1:c.1459+65C= NP_000120.2:n.1459+65C=
XM_006715010.2:c.1459+65C= XP_006715073.1:n.1459+65C=
XM_011514342.1:c.1621+65C= XP_011512644.1:n.1621+65C=
NM_000129.4:c.1459+65C= MANE Select NP_000120.2:n.1459+65C=
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