Canonical Allele Identifier: CA3970739
Community Standard Title: NM_001010892.3(RSPH4A):c.287C>T (p.Pro96Leu)
Gene: RSPH4A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.116616910C>T , CM000668.2:g.116616910C>T GRCh38
NC_000006.11:g.116938073C>T , CM000668.1:g.116938073C>T GRCh37
NC_000006.10:g.117044766C>T NCBI36
NG_012934.1:g.5432C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001010892.3:c.287C>T MANE Select NP_001010892.1:p.Pro96Leu
ENST00000229554.10:c.287C>T MANE Select ENSP00000229554.5:p.Pro96Leu
NM_001010892.2:c.287C>T NP_001010892.1:p.Pro96Leu
NM_001161664.1:c.287C>T NP_001155136.1:p.Pro96Leu
NM_001161664.2:c.287C>T NP_001155136.1:p.Pro96Leu
ENST00000229554.9:c.287C>T ENSP00000229554.5:p.Pro96Leu
ENST00000368580.4:c.287C>T ENSP00000357569.4:p.Pro96Leu
ENST00000368581.8:c.287C>T ENSP00000357570.4:p.Pro96Leu
XM_006715469.2:c.287C>T XP_006715532.1:p.Pro96Leu
XM_011535791.1:c.287C>T XP_011534093.1:p.Pro96Leu
XM_011535792.1:c.287C>T XP_011534094.1:p.Pro96Leu
XM_017010826.1:c.287C>T XP_016866315.1:p.Pro96Leu
XR_942416.1:n.2938C>T