Canonical Allele Identifier: CA3971123
Community Standard Title: NM_001010892.3(RSPH4A):c.2135A>G (p.Glu712Gly)
Gene: RSPH4A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.116632425A>G , CM000668.2:g.116632425A>G GRCh38
NC_000006.11:g.116953588A>G , CM000668.1:g.116953588A>G GRCh37
NC_000006.10:g.117060281A>G NCBI36
NG_012934.1:g.20947A>G

Transcript Alleles

HGVS Amino-acid Change
NM_001010892.3:c.2135A>G MANE Select NP_001010892.1:p.Glu712Gly
ENST00000229554.10:c.2135A>G MANE Select ENSP00000229554.5:p.Glu712Gly
NM_001010892.2:c.2135A>G NP_001010892.1:p.Glu712Gly
NM_001161664.1:c.*196A>G NP_001155136.1:n.*196A>G
NM_001161664.2:c.*196A>G NP_001155136.1:n.*196A>G
ENST00000229554.9:c.2135A>G ENSP00000229554.5:p.Glu712Gly
ENST00000368580.4:c.1394A>G ENSP00000357569.4:p.Glu465Gly
ENST00000368581.8:c.*196A>G ENSP00000357570.4:n.*196A>G
XM_006715469.2:c.*196A>G XP_006715532.1:n.*196A>G
XM_011535791.1:c.2135A>G XP_011534093.1:p.Glu712Gly
XM_011535792.1:c.2135A>G XP_011534094.1:p.Glu712Gly
XM_017010826.1:c.*196A>G XP_016866315.1:n.*196A>G