Canonical Allele Identifier: CA1697470619

Gene: SCRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.29922752C= , CM000669.2:g.29922752C=	GRCh38
NC_000007.13:g.29962368C= , CM000669.1:g.29962368C=	GRCh37
NC_000007.12:g.29928893C=	NCBI36
NG_047114.1:g.72538G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242059.10:c.*1205G= MANE Select	ENSP00000242059.5:n.*1205G=
ENST00000242059.9:c.*1205G=	ENSP00000242059.5:n.*1205G=
ENST00000426154.5:c.*1205G=	ENSP00000409068.1:n.*1205G=
NM_001145513.1:c.*1205G=	NP_001138985.1:n.*1205G=
NM_001145514.1:c.*1205G=	NP_001138986.1:n.*1205G=
NM_001145515.1:c.*1205G=	NP_001138987.1:n.*1205G=
NM_014766.4:c.*1205G=	NP_055581.3:n.*1205G=
XM_005249918.3:c.*1205G=	XP_005249975.1:n.*1205G=
XM_011515653.1:c.*1205G=	XP_011513955.1:n.*1205G=
XM_024447007.1:c.*1205G=	XP_024302775.1:n.*1205G=
NM_014766.5:c.*1205G= MANE Select	NP_055581.3:n.*1205G=
NM_001145515.2:c.*1205G=	NP_001138987.1:n.*1205G=