Canonical Allele Identifier: CA2680118080

Gene: RSPH4A

Linked Data

• gnomAD v4: 6-116627600-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.116627600A>T , CM000668.2:g.116627600A>T	GRCh38
NC_000006.11:g.116948763A>T , CM000668.1:g.116948763A>T	GRCh37
NC_000006.10:g.117055456A>T	NCBI36
NG_012934.1:g.16122A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229554.10:c.922-29A>T MANE Select	ENSP00000229554.5:n.922-29A>T
ENST00000229554.9:c.922-29A>T	ENSP00000229554.5:n.922-29A>T
ENST00000368580.4:c.922-1967A>T	ENSP00000357569.4:n.922-1967A>T
ENST00000368581.8:c.922-29A>T	ENSP00000357570.4:n.922-29A>T
NM_001010892.2:c.922-29A>T	NP_001010892.1:n.922-29A>T
NM_001161664.1:c.922-29A>T	NP_001155136.1:n.922-29A>T
XM_006715469.2:c.922-29A>T	XP_006715532.1:n.922-29A>T
XM_011535791.1:c.922-29A>T	XP_011534093.1:n.922-29A>T
XM_011535792.1:c.922-29A>T	XP_011534094.1:n.922-29A>T
XR_942416.1:n.3573-29A>T
XM_017010826.1:c.922-29A>T	XP_016866315.1:n.922-29A>T
NM_001010892.3:c.922-29A>T MANE Select	NP_001010892.1:n.922-29A>T
NM_001161664.2:c.922-29A>T	NP_001155136.1:n.922-29A>T