Canonical Allele Identifier: CA3970894
Community Standard Title: NM_001010892.3(RSPH4A):c.1082G>T (p.Gly361Val)
Gene: RSPH4A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.116627789G>T , CM000668.2:g.116627789G>T GRCh38
NC_000006.11:g.116948952G>T , CM000668.1:g.116948952G>T GRCh37
NC_000006.10:g.117055645G>T NCBI36
NG_012934.1:g.16311G>T

Transcript Alleles

HGVS Amino-acid Change
NM_001010892.3:c.1082G>T MANE Select NP_001010892.1:p.Gly361Val
ENST00000229554.10:c.1082G>T MANE Select ENSP00000229554.5:p.Gly361Val
NM_001010892.2:c.1082G>T NP_001010892.1:p.Gly361Val
NM_001161664.1:c.1082G>T NP_001155136.1:p.Gly361Val
NM_001161664.2:c.1082G>T NP_001155136.1:p.Gly361Val
ENST00000229554.9:c.1082G>T ENSP00000229554.5:p.Gly361Val
ENST00000368580.4:c.922-1778G>T ENSP00000357569.4:n.922-1778G>T
ENST00000368581.8:c.1082G>T ENSP00000357570.4:p.Gly361Val
XM_006715469.2:c.1082G>T XP_006715532.1:p.Gly361Val
XM_011535791.1:c.1082G>T XP_011534093.1:p.Gly361Val
XM_011535792.1:c.1082G>T XP_011534094.1:p.Gly361Val
XM_017010826.1:c.1082G>T XP_016866315.1:p.Gly361Val
XR_942416.1:n.3733G>T