Canonical Allele Identifier: CA2772740998

Gene: RSPH4A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.116617039_116617040insAAACACAC , CM000668.2:g.116617039_116617040insAAACACAC	GRCh38
NC_000006.11:g.116938202_116938203insAAACACAC , CM000668.1:g.116938202_116938203insAAACACAC	GRCh37
NC_000006.10:g.117044895_117044896insAAACACAC	NCBI36
NG_012934.1:g.5561_5562insAAACACAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229554.10:c.416_417insAAACACAC MANE Select	ENSP00000229554.5:p.His140AsnfsTer30
ENST00000229554.9:c.416_417insAAACACAC	ENSP00000229554.5:p.His140AsnfsTer30
ENST00000368580.4:c.416_417insAAACACAC	ENSP00000357569.4:p.His140AsnfsTer30
ENST00000368581.8:c.416_417insAAACACAC	ENSP00000357570.4:p.His140AsnfsTer30
NM_001010892.2:c.416_417insAAACACAC	NP_001010892.1:p.His140AsnfsTer30
NM_001161664.1:c.416_417insAAACACAC	NP_001155136.1:p.His140AsnfsTer30
XM_006715469.2:c.416_417insAAACACAC	XP_006715532.1:p.His140AsnfsTer30
XM_011535791.1:c.416_417insAAACACAC	XP_011534093.1:p.His140AsnfsTer30
XM_011535792.1:c.416_417insAAACACAC	XP_011534094.1:p.His140AsnfsTer30
XR_942416.1:n.3067_3068insAAACACAC
XM_017010826.1:c.416_417insAAACACAC	XP_016866315.1:p.His140AsnfsTer30
NM_001010892.3:c.416_417insAAACACAC MANE Select	NP_001010892.1:p.His140AsnfsTer30
NM_001161664.2:c.416_417insAAACACAC	NP_001155136.1:p.His140AsnfsTer30