Canonical Allele Identifier: CA3970682

Gene: RSPH4A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.116616611T>A , CM000668.2:g.116616611T>A	GRCh38
NC_000006.11:g.116937774T>A , CM000668.1:g.116937774T>A	GRCh37
NC_000006.10:g.117044467T>A	NCBI36
NG_012934.1:g.5133T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001010892.3:c.-13T>A MANE Select	NP_001010892.1:n.-13T>A
ENST00000229554.10:c.-13T>A MANE Select	ENSP00000229554.5:n.-13T>A
NM_001010892.2:c.-13T>A	NP_001010892.1:n.-13T>A
NM_001161664.1:c.-13T>A	NP_001155136.1:n.-13T>A
NM_001161664.2:c.-13T>A	NP_001155136.1:n.-13T>A
ENST00000229554.9:c.-13T>A	ENSP00000229554.5:n.-13T>A
ENST00000368581.8:c.-13T>A	ENSP00000357570.4:n.-13T>A
XM_006715469.2:c.-13T>A	XP_006715532.1:n.-13T>A
XM_011535791.1:c.-13T>A	XP_011534093.1:n.-13T>A
XM_011535792.1:c.-13T>A	XP_011534094.1:n.-13T>A
XM_017010826.1:c.-13T>A	XP_016866315.1:n.-13T>A
XR_942416.1:n.2639T>A