Canonical Allele Identifier: CA1607949747
Gene: F13A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6145495C= , CM000668.2:g.6145495C= GRCh38
NC_000006.11:g.6145728C= , CM000668.1:g.6145728C= GRCh37
NC_000006.10:g.6090727C= NCBI36
NG_008107.1:g.180197G= , LRG_549:g.180197G=

Transcript Alleles

HGVS Amino-acid change
ENST00000264870.8:c.*124G= MANE Select ENSP00000264870.3:n.*124G=
ENST00000264870.7:c.*124G= ENSP00000264870.3:n.*124G=
NM_000129.3:c.*124G= , LRG_549t1:c.*124G= NP_000120.2:n.*124G=
XM_006715010.2:c.*124G= XP_006715073.1:n.*124G=
XM_011514342.1:c.*124G= XP_011512644.1:n.*124G=
NM_000129.4:c.*124G= MANE Select NP_000120.2:n.*124G=