Canonical Allele Identifier: CA365413352

Gene: RSPH4A

Linked Data

• MyVariant Identifiers: chr6:g.116953522G>C (hg19) ; chr6:g.116632359G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.116632359G>C , CM000668.2:g.116632359G>C	GRCh38
NC_000006.11:g.116953522G>C , CM000668.1:g.116953522G>C	GRCh37
NC_000006.10:g.117060215G>C	NCBI36
NG_012934.1:g.20881G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229554.10:c.2069G>C MANE Select	ENSP00000229554.5:p.Arg690Thr
ENST00000229554.9:c.2069G>C	ENSP00000229554.5:p.Arg690Thr
ENST00000368580.4:c.1328G>C	ENSP00000357569.4:p.Arg443Thr
ENST00000368581.8:c.*130G>C	ENSP00000357570.4:n.*130G>C
NM_001010892.2:c.2069G>C	NP_001010892.1:p.Arg690Thr
NM_001161664.1:c.*130G>C	NP_001155136.1:n.*130G>C
XM_006715469.2:c.*130G>C	XP_006715532.1:n.*130G>C
XM_011535791.1:c.2069G>C	XP_011534093.1:p.Arg690Thr
XM_011535792.1:c.2069G>C	XP_011534094.1:p.Arg690Thr
XM_017010826.1:c.*130G>C	XP_016866315.1:n.*130G>C
NM_001010892.3:c.2069G>C MANE Select	NP_001010892.1:p.Arg690Thr
NM_001161664.2:c.*130G>C	NP_001155136.1:n.*130G>C