Canonical Allele Identifier: CA1593016446
Gene: MRPL22 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154969023C= , CM000667.2:g.154969023C= GRCh38
NC_000005.9:g.154348583C= , CM000667.1:g.154348583C= GRCh37
NC_000005.8:g.154328776C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000523037.6:c.*2126C= MANE Select ENSP00000431040.1:n.*2126C=
ENST00000265229.12:c.*2126C= ENSP00000265229.8:n.*2126C=
ENST00000522038.5:c.*2126C= ENSP00000429039.1:n.*2126C=
ENST00000523037.5:c.*2126C= ENSP00000431040.1:n.*2126C=
NM_001014990.2:c.*2126C= NP_001014990.1:n.*2126C=
NM_014180.3:c.*2126C= NP_054899.2:n.*2126C=
NM_014180.4:c.*2126C= MANE Select NP_054899.2:n.*2126C=
NM_001014990.3:c.*2126C= NP_001014990.1:n.*2126C=
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