Canonical Allele Identifier: CA145927041

Gene: RSPH4A

Linked Data

• dbSNP Id: rs777389220
• MyVariant Identifiers: chr6:g.116948850T>C (hg19) ; chr6:g.116627687T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.116627687T>C , CM000668.2:g.116627687T>C	GRCh38
NC_000006.11:g.116948850T>C , CM000668.1:g.116948850T>C	GRCh37
NC_000006.10:g.117055543T>C	NCBI36
NG_012934.1:g.16209T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000229554.10:c.980T>C MANE Select	ENSP00000229554.5:p.Val327Ala
ENST00000229554.9:c.980T>C	ENSP00000229554.5:p.Val327Ala
ENST00000368580.4:c.922-1880T>C	ENSP00000357569.4:n.922-1880T>C
ENST00000368581.8:c.980T>C	ENSP00000357570.4:p.Val327Ala
NM_001010892.2:c.980T>C	NP_001010892.1:p.Val327Ala
NM_001161664.1:c.980T>C	NP_001155136.1:p.Val327Ala
XM_006715469.2:c.980T>C	XP_006715532.1:p.Val327Ala
XM_011535791.1:c.980T>C	XP_011534093.1:p.Val327Ala
XM_011535792.1:c.980T>C	XP_011534094.1:p.Val327Ala
XR_942416.1:n.3631T>C
XM_017010826.1:c.980T>C	XP_016866315.1:p.Val327Ala
NM_001010892.3:c.980T>C MANE Select	NP_001010892.1:p.Val327Ala
NM_001161664.2:c.980T>C	NP_001155136.1:p.Val327Ala