Canonical Allele Identifier: CA365392294

Gene: RSPH4A

Linked Data

• dbSNP Id: rs1775516975
• MyVariant Identifiers: chr6:g.116938151C>T (hg19) ; chr6:g.116616988C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.116616988C>T , CM000668.2:g.116616988C>T	GRCh38
NC_000006.11:g.116938151C>T , CM000668.1:g.116938151C>T	GRCh37
NC_000006.10:g.117044844C>T	NCBI36
NG_012934.1:g.5510C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229554.10:c.365C>T MANE Select	ENSP00000229554.5:p.Thr122Ile
ENST00000229554.9:c.365C>T	ENSP00000229554.5:p.Thr122Ile
ENST00000368580.4:c.365C>T	ENSP00000357569.4:p.Thr122Ile
ENST00000368581.8:c.365C>T	ENSP00000357570.4:p.Thr122Ile
NM_001010892.2:c.365C>T	NP_001010892.1:p.Thr122Ile
NM_001161664.1:c.365C>T	NP_001155136.1:p.Thr122Ile
XM_006715469.2:c.365C>T	XP_006715532.1:p.Thr122Ile
XM_011535791.1:c.365C>T	XP_011534093.1:p.Thr122Ile
XM_011535792.1:c.365C>T	XP_011534094.1:p.Thr122Ile
XR_942416.1:n.3016C>T
XM_017010826.1:c.365C>T	XP_016866315.1:p.Thr122Ile
NM_001010892.3:c.365C>T MANE Select	NP_001010892.1:p.Thr122Ile
NM_001161664.2:c.365C>T	NP_001155136.1:p.Thr122Ile