Canonical Allele Identifier: CA365392815

Gene: RSPH4A

Linked Data

• gnomAD v4: 6-116617024-A-C
• MyVariant Identifiers: chr6:g.116938187A>C (hg19) ; chr6:g.116617024A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.116617024A>C , CM000668.2:g.116617024A>C	GRCh38
NC_000006.11:g.116938187A>C , CM000668.1:g.116938187A>C	GRCh37
NC_000006.10:g.117044880A>C	NCBI36
NG_012934.1:g.5546A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229554.10:c.401A>C MANE Select	ENSP00000229554.5:p.Lys134Thr
ENST00000229554.9:c.401A>C	ENSP00000229554.5:p.Lys134Thr
ENST00000368580.4:c.401A>C	ENSP00000357569.4:p.Lys134Thr
ENST00000368581.8:c.401A>C	ENSP00000357570.4:p.Lys134Thr
NM_001010892.2:c.401A>C	NP_001010892.1:p.Lys134Thr
NM_001161664.1:c.401A>C	NP_001155136.1:p.Lys134Thr
XM_006715469.2:c.401A>C	XP_006715532.1:p.Lys134Thr
XM_011535791.1:c.401A>C	XP_011534093.1:p.Lys134Thr
XM_011535792.1:c.401A>C	XP_011534094.1:p.Lys134Thr
XR_942416.1:n.3052A>C
XM_017010826.1:c.401A>C	XP_016866315.1:p.Lys134Thr
NM_001010892.3:c.401A>C MANE Select	NP_001010892.1:p.Lys134Thr
NM_001161664.2:c.401A>C	NP_001155136.1:p.Lys134Thr