Canonical Allele Identifier: CA1697470820

Gene: SCRN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.29922994_29922998delinsCTAAA , CM000669.2:g.29922994_29922998delinsCTAAA	GRCh38
NC_000007.13:g.29962610_29962614delinsCTAAA , CM000669.1:g.29962610_29962614delinsCTAAA	GRCh37
NC_000007.12:g.29929135_29929139delinsCTAAA	NCBI36
NG_047114.1:g.72292_72296delinsTTTAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242059.10:c.*959_*963delinsTTTAG MANE Select	ENSP00000242059.5:n.*959_*963delinsTTTAG
ENST00000242059.9:c.*959_*963delinsTTTAG	ENSP00000242059.5:n.*959_*963delinsTTTAG
ENST00000426154.5:c.*959_*963delinsTTTAG	ENSP00000409068.1:n.*959_*963delinsTTTAG
NM_001145513.1:c.*959_*963delinsTTTAG	NP_001138985.1:n.*959_*963delinsTTTAG
NM_001145514.1:c.*959_*963delinsTTTAG	NP_001138986.1:n.*959_*963delinsTTTAG
NM_001145515.1:c.*959_*963delinsTTTAG	NP_001138987.1:n.*959_*963delinsTTTAG
NM_014766.4:c.*959_*963delinsTTTAG	NP_055581.3:n.*959_*963delinsTTTAG
XM_005249918.3:c.*959_*963delinsTTTAG	XP_005249975.1:n.*959_*963delinsTTTAG
XM_011515653.1:c.*959_*963delinsTTTAG	XP_011513955.1:n.*959_*963delinsTTTAG
XM_024447007.1:c.*959_*963delinsTTTAG	XP_024302775.1:n.*959_*963delinsTTTAG
NM_014766.5:c.*959_*963delinsTTTAG MANE Select	NP_055581.3:n.*959_*963delinsTTTAG
NM_001145515.2:c.*959_*963delinsTTTAG	NP_001138987.1:n.*959_*963delinsTTTAG