Canonical Allele Identifier: CA1697470900

Gene: SCRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.29923080_29923081delinsTC , CM000669.2:g.29923080_29923081delinsTC	GRCh38
NC_000007.13:g.29962696_29962697delinsTC , CM000669.1:g.29962696_29962697delinsTC	GRCh37
NC_000007.12:g.29929221_29929222delinsTC	NCBI36
NG_047114.1:g.72209_72210delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242059.10:c.*876_*877delinsGA MANE Select	ENSP00000242059.5:n.*876_*877delinsGA
ENST00000242059.9:c.*876_*877delinsGA	ENSP00000242059.5:n.*876_*877delinsGA
ENST00000426154.5:c.*876_*877delinsGA	ENSP00000409068.1:n.*876_*877delinsGA
NM_001145513.1:c.*876_*877delinsGA	NP_001138985.1:n.*876_*877delinsGA
NM_001145514.1:c.*876_*877delinsGA	NP_001138986.1:n.*876_*877delinsGA
NM_001145515.1:c.*876_*877delinsGA	NP_001138987.1:n.*876_*877delinsGA
NM_014766.4:c.*876_*877delinsGA	NP_055581.3:n.*876_*877delinsGA
XM_005249918.3:c.*876_*877delinsGA	XP_005249975.1:n.*876_*877delinsGA
XM_011515653.1:c.*876_*877delinsGA	XP_011513955.1:n.*876_*877delinsGA
XM_024447007.1:c.*876_*877delinsGA	XP_024302775.1:n.*876_*877delinsGA
NM_014766.5:c.*876_*877delinsGA MANE Select	NP_055581.3:n.*876_*877delinsGA
NM_001145515.2:c.*876_*877delinsGA	NP_001138987.1:n.*876_*877delinsGA