Canonical Allele Identifier: CA1607949439
Gene: F13A1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.6144712_6144713delinsTG , CM000668.2:g.6144712_6144713delinsTG GRCh38
NC_000006.11:g.6144945_6144946delinsTG , CM000668.1:g.6144945_6144946delinsTG GRCh37
NC_000006.10:g.6089944_6089945delinsTG NCBI36
NG_008107.1:g.180979_180980delinsCA , LRG_549:g.180979_180980delinsCA

Transcript Alleles

HGVS Amino-acid change
ENST00000264870.8:c.*906_*907delinsCA MANE Select ENSP00000264870.3:n.*906_*907delinsCA
ENST00000264870.7:c.*906_*907delinsCA ENSP00000264870.3:n.*906_*907delinsCA
NM_000129.3:c.*906_*907delinsCA , LRG_549t1:c.*906_*907delinsCA NP_000120.2:n.*906_*907delinsCA
XM_006715010.2:c.*906_*907delinsCA XP_006715073.1:n.*906_*907delinsCA
XM_011514342.1:c.*906_*907delinsCA XP_011512644.1:n.*906_*907delinsCA
NM_000129.4:c.*906_*907delinsCA MANE Select NP_000120.2:n.*906_*907delinsCA
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