Canonical Allele Identifier: CA1593016440
Gene: MRPL22 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154969019T= , CM000667.2:g.154969019T= GRCh38
NC_000005.9:g.154348579T= , CM000667.1:g.154348579T= GRCh37
NC_000005.8:g.154328772T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000523037.6:c.*2122T= MANE Select ENSP00000431040.1:n.*2122T=
ENST00000265229.12:c.*2122T= ENSP00000265229.8:n.*2122T=
ENST00000522038.5:c.*2122T= ENSP00000429039.1:n.*2122T=
ENST00000523037.5:c.*2122T= ENSP00000431040.1:n.*2122T=
NM_001014990.2:c.*2122T= NP_001014990.1:n.*2122T=
NM_014180.3:c.*2122T= NP_054899.2:n.*2122T=
NM_014180.4:c.*2122T= MANE Select NP_054899.2:n.*2122T=
NM_001014990.3:c.*2122T= NP_001014990.1:n.*2122T=