Canonical Allele Identifier: CA1607949735
Gene: F13A1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6145476_6145477delinsTG , CM000668.2:g.6145476_6145477delinsTG GRCh38
NC_000006.11:g.6145709_6145710delinsTG , CM000668.1:g.6145709_6145710delinsTG GRCh37
NC_000006.10:g.6090708_6090709delinsTG NCBI36
NG_008107.1:g.180215_180216delinsCA , LRG_549:g.180215_180216delinsCA

Transcript Alleles

HGVS Amino-acid change
ENST00000264870.8:c.*142_*143delinsCA MANE Select ENSP00000264870.3:n.*142_*143delinsCA
ENST00000264870.7:c.*142_*143delinsCA ENSP00000264870.3:n.*142_*143delinsCA
NM_000129.3:c.*142_*143delinsCA , LRG_549t1:c.*142_*143delinsCA NP_000120.2:n.*142_*143delinsCA
XM_006715010.2:c.*142_*143delinsCA XP_006715073.1:n.*142_*143delinsCA
XM_011514342.1:c.*142_*143delinsCA XP_011512644.1:n.*142_*143delinsCA
NM_000129.4:c.*142_*143delinsCA MANE Select NP_000120.2:n.*142_*143delinsCA
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