Canonical Allele Identifier: CA14755520
Gene: RALY HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.34077942A>G , CM000682.2:g.34077942A>G GRCh38
NC_000020.10:g.32665748A>G , CM000682.1:g.32665748A>G GRCh37
NC_000020.9:g.32129409A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000246194.8:c.877-563A>G MANE Select ENSP00000246194.3:n.877-563A>G
ENST00000246194.7:c.877-563A>G ENSP00000246194.3:n.877-563A>G
ENST00000375114.7:c.829-563A>G ENSP00000364255.3:n.829-563A>G
ENST00000489384.1:n.34-563A>G
NM_007367.3:c.829-563A>G NP_031393.2:n.829-563A>G
NM_016732.2:c.877-563A>G NP_057951.1:n.877-563A>G
XM_005260334.3:c.877-563A>G XP_005260391.1:n.877-563A>G
XM_005260336.3:c.829-563A>G XP_005260393.1:n.829-563A>G
XM_011528694.1:c.877-563A>G XP_011526996.1:n.877-563A>G
XM_011528695.1:c.877-563A>G XP_011526997.1:n.877-563A>G
XM_005260334.5:c.877-563A>G XP_005260391.1:n.877-563A>G
XM_005260336.5:c.829-563A>G XP_005260393.1:n.829-563A>G
XM_011528694.3:c.877-563A>G XP_011526996.1:n.877-563A>G
XM_011528695.3:c.877-563A>G XP_011526997.1:n.877-563A>G
XM_017027731.2:c.877-563A>G XP_016883220.1:n.877-563A>G
XM_024451857.1:c.877-563A>G XP_024307625.1:n.877-563A>G
XM_024451858.1:c.877-563A>G XP_024307626.1:n.877-563A>G
XM_024451859.1:c.877-563A>G XP_024307627.1:n.877-563A>G
NM_016732.3:c.877-563A>G MANE Select NP_057951.1:n.877-563A>G
NM_007367.4:c.829-563A>G NP_031393.2:n.829-563A>G
Search 100 bp 5'
Search 100 bp 3'