Canonical Allele Identifier: CA1697470847

Gene: SCRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.29923037_29923038delinsAG , CM000669.2:g.29923037_29923038delinsAG	GRCh38
NC_000007.13:g.29962653_29962654delinsAG , CM000669.1:g.29962653_29962654delinsAG	GRCh37
NC_000007.12:g.29929178_29929179delinsAG	NCBI36
NG_047114.1:g.72252_72253delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242059.10:c.*919_*920delinsCT MANE Select	ENSP00000242059.5:n.*919_*920delinsCT
ENST00000242059.9:c.*919_*920delinsCT	ENSP00000242059.5:n.*919_*920delinsCT
ENST00000426154.5:c.*919_*920delinsCT	ENSP00000409068.1:n.*919_*920delinsCT
NM_001145513.1:c.*919_*920delinsCT	NP_001138985.1:n.*919_*920delinsCT
NM_001145514.1:c.*919_*920delinsCT	NP_001138986.1:n.*919_*920delinsCT
NM_001145515.1:c.*919_*920delinsCT	NP_001138987.1:n.*919_*920delinsCT
NM_014766.4:c.*919_*920delinsCT	NP_055581.3:n.*919_*920delinsCT
XM_005249918.3:c.*919_*920delinsCT	XP_005249975.1:n.*919_*920delinsCT
XM_011515653.1:c.*919_*920delinsCT	XP_011513955.1:n.*919_*920delinsCT
XM_024447007.1:c.*919_*920delinsCT	XP_024302775.1:n.*919_*920delinsCT
NM_014766.5:c.*919_*920delinsCT MANE Select	NP_055581.3:n.*919_*920delinsCT
NM_001145515.2:c.*919_*920delinsCT	NP_001138987.1:n.*919_*920delinsCT