Canonical Allele Identifier: CA1676375762

Gene: RSPH3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158982405A= , CM000668.2:g.158982405A=	GRCh38
NC_000006.11:g.159403437A= , CM000668.1:g.159403437A=	GRCh37
NC_000006.10:g.159323425A=	NCBI36
NG_051819.1:g.22783T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367069.7:c.696+80T= MANE Select	ENSP00000356036.1:n.696+80T=
ENST00000252655.1:c.1122+80T=	ENSP00000252655.1:n.1122+80T=
ENST00000367069.6:c.696+80T=	ENSP00000356036.1:n.696+80T=
ENST00000449822.5:c.408+80T=	ENSP00000393195.1:n.408+80T=
NM_031924.4:c.1122+80T=	NP_114130.3:n.1122+80T=
XM_005267153.3:c.834+80T=	XP_005267210.1:n.834+80T=
XR_245553.2:n.1578+80T=
NM_001346418.1:c.834+80T=	NP_001333347.1:n.834+80T=
NM_031924.5:c.1122+80T=	NP_114130.3:n.1122+80T=
NR_144434.1:n.1333+80T=
XM_017011347.2:c.306+80T=	XP_016866836.1:n.306+80T=
XM_024446566.1:c.306+80T=	XP_024302334.1:n.306+80T=
XR_001743668.2:n.1572+80T=
XR_001743669.2:n.1572+80T=
XR_001743670.2:n.1284+80T=
XR_001743671.2:n.778+80T=
NM_031924.6:c.1122+80T=	NP_114130.3:n.1122+80T=
NM_031924.8:c.696+80T= MANE Select	NP_114130.4:n.696+80T=