Canonical Allele Identifier: CA2677188820
Gene: F13A1 HGNC NCBI

Linked Data

gnomAD v4: 6-6144680-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6144680G>A , CM000668.2:g.6144680G>A GRCh38
NC_000006.11:g.6144913G>A , CM000668.1:g.6144913G>A GRCh37
NC_000006.10:g.6089912G>A NCBI36
NG_008107.1:g.181012C>T , LRG_549:g.181012C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264870.8:c.*939C>T MANE Select ENSP00000264870.3:n.*939C>T
ENST00000264870.7:c.*939C>T ENSP00000264870.3:n.*939C>T
NM_000129.3:c.*939C>T , LRG_549t1:c.*939C>T NP_000120.2:n.*939C>T
XM_006715010.2:c.*939C>T XP_006715073.1:n.*939C>T
XM_011514342.1:c.*939C>T XP_011512644.1:n.*939C>T
NM_000129.4:c.*939C>T MANE Select NP_000120.2:n.*939C>T
Search 100 bp 5'
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