Canonical Allele Identifier: CA2336378182
Gene: AXL HGNC NCBI

Linked Data

dbSNP Id: rs2034352043
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41250924T>C , CM000681.2:g.41250924T>C GRCh38
NC_000019.9:g.41756829T>C , CM000681.1:g.41756829T>C GRCh37
NC_000019.8:g.46448669T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000301178.9:c.1712-1427T>C MANE Select ENSP00000301178.3:n.1712-1427T>C
ENST00000301178.8:c.1712-1427T>C ENSP00000301178.3:n.1712-1427T>C
ENST00000359092.7:c.1685-1427T>C ENSP00000351995.2:n.1685-1427T>C
ENST00000593513.1:c.908-1427T>C ENSP00000471497.1:n.908-1427T>C
NM_001278599.1:c.908-1427T>C NP_001265528.1:n.908-1427T>C
NM_001699.5:c.1685-1427T>C NP_001690.2:n.1685-1427T>C
NM_021913.4:c.1712-1427T>C NP_068713.2:n.1712-1427T>C
NM_021913.5:c.1712-1427T>C MANE Select NP_068713.2:n.1712-1427T>C
NM_001699.6:c.1685-1427T>C NP_001690.2:n.1685-1427T>C
NM_001278599.2:c.908-1427T>C NP_001265528.1:n.908-1427T>C
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