Canonical Allele Identifier: CA410364837
Community Standard Title: NM_080860.4(RSPH1):c.502-1G>A
Gene: RSPH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.42482709C>T , CM000683.2:g.42482709C>T GRCh38
NC_000021.8:g.43902819C>T , CM000683.1:g.43902819C>T GRCh37
NC_000021.7:g.42775888C>T NCBI36
NG_034257.1:g.18646G>A

Transcript Alleles

HGVS Amino-acid Change
NM_080860.4:c.502-1G>A MANE Select NP_543136.1:n.502-1G>A
ENST00000291536.8:c.502-1G>A MANE Select ENSP00000291536.3:n.502-1G>A
NM_001286506.1:c.388-1G>A NP_001273435.1:n.388-1G>A
NM_001286506.2:c.388-1G>A NP_001273435.1:n.388-1G>A
NM_080860.3:c.502-1G>A NP_543136.1:n.502-1G>A
ENST00000291536.7:c.502-1G>A ENSP00000291536.3:n.502-1G>A
ENST00000398352.3:c.388-1G>A ENSP00000381395.3:n.388-1G>A
ENST00000493019.1:n.2120-1G>A
XM_005261208.1:c.295-1G>A XP_005261265.1:n.295-1G>A
XM_005261208.2:c.295-1G>A XP_005261265.1:n.295-1G>A
XM_011529786.1:c.501+2960G>A XP_011528088.1:n.501+2960G>A