Canonical Allele Identifier: CA570038160

Gene: RSPH4A

Linked Data

• dbSNP Id: rs1214873033
• gnomAD v2: 6-116948786-C-G
• gnomAD v4: 6-116627623-C-G
• MyVariant Identifiers: chr6:g.116948786C>G (hg19) ; chr6:g.116627623C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.116627623C>G , CM000668.2:g.116627623C>G	GRCh38
NC_000006.11:g.116948786C>G , CM000668.1:g.116948786C>G	GRCh37
NC_000006.10:g.117055479C>G	NCBI36
NG_012934.1:g.16145C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229554.10:c.922-6C>G MANE Select	ENSP00000229554.5:n.922-6C>G
ENST00000229554.9:c.922-6C>G	ENSP00000229554.5:n.922-6C>G
ENST00000368580.4:c.922-1944C>G	ENSP00000357569.4:n.922-1944C>G
ENST00000368581.8:c.922-6C>G	ENSP00000357570.4:n.922-6C>G
NM_001010892.2:c.922-6C>G	NP_001010892.1:n.922-6C>G
NM_001161664.1:c.922-6C>G	NP_001155136.1:n.922-6C>G
XM_006715469.2:c.922-6C>G	XP_006715532.1:n.922-6C>G
XM_011535791.1:c.922-6C>G	XP_011534093.1:n.922-6C>G
XM_011535792.1:c.922-6C>G	XP_011534094.1:n.922-6C>G
XR_942416.1:n.3573-6C>G
XM_017010826.1:c.922-6C>G	XP_016866315.1:n.922-6C>G
NM_001010892.3:c.922-6C>G MANE Select	NP_001010892.1:n.922-6C>G
NM_001161664.2:c.922-6C>G	NP_001155136.1:n.922-6C>G