Canonical Allele Identifier: CA365413319

Gene: RSPH4A

Linked Data

• MyVariant Identifiers: chr6:g.116953515G>A (hg19) ; chr6:g.116632352G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.116632352G>A , CM000668.2:g.116632352G>A	GRCh38
NC_000006.11:g.116953515G>A , CM000668.1:g.116953515G>A	GRCh37
NC_000006.10:g.117060208G>A	NCBI36
NG_012934.1:g.20874G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229554.10:c.2062G>A MANE Select	ENSP00000229554.5:p.Ala688Thr
ENST00000229554.9:c.2062G>A	ENSP00000229554.5:p.Ala688Thr
ENST00000368580.4:c.1321G>A	ENSP00000357569.4:p.Ala441Thr
ENST00000368581.8:c.*123G>A	ENSP00000357570.4:n.*123G>A
NM_001010892.2:c.2062G>A	NP_001010892.1:p.Ala688Thr
NM_001161664.1:c.*123G>A	NP_001155136.1:n.*123G>A
XM_006715469.2:c.*123G>A	XP_006715532.1:n.*123G>A
XM_011535791.1:c.2062G>A	XP_011534093.1:p.Ala688Thr
XM_011535792.1:c.2062G>A	XP_011534094.1:p.Ala688Thr
XM_017010826.1:c.*123G>A	XP_016866315.1:n.*123G>A
NM_001010892.3:c.2062G>A MANE Select	NP_001010892.1:p.Ala688Thr
NM_001161664.2:c.*123G>A	NP_001155136.1:n.*123G>A