Canonical Allele Identifier: CA287551789

Gene: AURKB

Linked Data

• gnomAD v4: 17-8204737-G-T
• MyVariant Identifiers: chr17:g.8108055G>T (hg19) ; chr17:g.8204737G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8204737G>T , CM000679.2:g.8204737G>T	GRCh38
NC_000017.10:g.8108055G>T , CM000679.1:g.8108055G>T	GRCh37
NC_000017.9:g.8048780G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585124.6:c.*134C>A MANE Select	ENSP00000463999.1:n.*134C>A
ENST00000316199.10:c.*134C>A	ENSP00000313950.6:n.*134C>A
NM_001256834.1:c.*134C>A	NP_001243763.1:n.*134C>A
NM_001256834.2:c.*134C>A	NP_001243763.1:n.*134C>A
NM_001284526.1:c.*134C>A	NP_001271455.1:n.*134C>A
NM_001313950.1:c.*134C>A	NP_001300879.1:n.*134C>A
NM_001313951.1:c.*134C>A	NP_001300880.1:n.*134C>A
NM_001313952.1:c.*134C>A	NP_001300881.1:n.*134C>A
NM_001313953.1:c.*134C>A	NP_001300882.1:n.*134C>A
NM_001313954.1:c.*134C>A	NP_001300883.1:n.*134C>A
NM_001313955.1:c.*134C>A	NP_001300884.1:n.*134C>A
NM_004217.3:c.*134C>A	NP_004208.2:n.*134C>A
NR_132730.1:n.1149C>A
NR_132731.1:n.1034C>A
XM_011524070.1:c.*134C>A	XP_011522372.1:n.*134C>A
XM_011524072.1:c.*134C>A	XP_011522374.1:n.*134C>A
NM_001313953.2:c.*134C>A	NP_001300882.1:n.*134C>A
XM_017025307.2:c.*134C>A	XP_016880796.1:n.*134C>A
NM_004217.4:c.*134C>A MANE Select	NP_004208.2:n.*134C>A
NM_001256834.3:c.*134C>A	NP_001243763.1:n.*134C>A
NM_001284526.2:c.*134C>A	NP_001271455.1:n.*134C>A
NM_001313950.2:c.*134C>A	NP_001300879.1:n.*134C>A
NM_001313952.2:c.*134C>A	NP_001300881.1:n.*134C>A
NM_001313953.3:c.*134C>A	NP_001300882.1:n.*134C>A
NM_001313954.2:c.*134C>A	NP_001300883.1:n.*134C>A
NM_001313955.2:c.*134C>A	NP_001300884.1:n.*134C>A
NR_132730.2:n.1098C>A