Canonical Allele Identifier: CA1607949692
Gene: F13A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6145366T= , CM000668.2:g.6145366T= GRCh38
NC_000006.11:g.6145599T= , CM000668.1:g.6145599T= GRCh37
NC_000006.10:g.6090598T= NCBI36
NG_008107.1:g.180326A= , LRG_549:g.180326A=

Transcript Alleles

HGVS Amino-acid change
ENST00000264870.8:c.*253A= MANE Select ENSP00000264870.3:n.*253A=
ENST00000264870.7:c.*253A= ENSP00000264870.3:n.*253A=
NM_000129.3:c.*253A= , LRG_549t1:c.*253A= NP_000120.2:n.*253A=
XM_006715010.2:c.*253A= XP_006715073.1:n.*253A=
XM_011514342.1:c.*253A= XP_011512644.1:n.*253A=
NM_000129.4:c.*253A= MANE Select NP_000120.2:n.*253A=