Canonical Allele Identifier: CA1607949422
Gene: F13A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6144677T= , CM000668.2:g.6144677T= GRCh38
NC_000006.11:g.6144910T= , CM000668.1:g.6144910T= GRCh37
NC_000006.10:g.6089909T= NCBI36
NG_008107.1:g.181015A= , LRG_549:g.181015A=

Transcript Alleles

HGVS Amino-acid change
ENST00000264870.8:c.*942A= MANE Select ENSP00000264870.3:n.*942A=
ENST00000264870.7:c.*942A= ENSP00000264870.3:n.*942A=
NM_000129.3:c.*942A= , LRG_549t1:c.*942A= NP_000120.2:n.*942A=
XM_006715010.2:c.*942A= XP_006715073.1:n.*942A=
XM_011514342.1:c.*942A= XP_011512644.1:n.*942A=
NM_000129.4:c.*942A= MANE Select NP_000120.2:n.*942A=