Canonical Allele Identifier: CA536617

Gene: SKI

Linked Data

• ClinVar Variation Id: 258899
• ClinVar RCV Id: RCV000248676 ; RCV002519914
• dbSNP Id: rs753878221
• ExAC: 1:2234856 C / T
• gnomAD v2: 1-2234856-C-T
• gnomAD v3: 1-2303417-C-T
• gnomAD v4: 1-2303417-C-T
• MyVariant Identifiers: chr1:g.2234856C>T (hg19) ; chr1:g.2303417C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2303417C>T , CM000663.2:g.2303417C>T	GRCh38
NC_000001.10:g.2234856C>T , CM000663.1:g.2234856C>T	GRCh37
NC_000001.9:g.2224716C>T	NCBI36
NG_013084.1:g.79723C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704337.1:n.379+17C>T
ENST00000378536.5:c.1211+17C>T MANE Select	ENSP00000367797.4:n.1211+17C>T
ENST00000378536.4:c.1211+17C>T	ENSP00000367797.4:n.1211+17C>T
NM_003036.3:c.1211+17C>T	NP_003027.1:n.1211+17C>T
XM_005244775.2:c.1211+17C>T	XP_005244832.1:n.1211+17C>T
XM_005244776.3:c.341+17C>T	XP_005244833.1:n.341+17C>T
XM_005244775.3:c.1211+17C>T	XP_005244832.1:n.1211+17C>T
XM_005244776.4:c.341+17C>T	XP_005244833.1:n.341+17C>T
XM_017002128.1:c.719+17C>T	XP_016857617.1:n.719+17C>T
NM_003036.4:c.1211+17C>T MANE Select	NP_003027.1:n.1211+17C>T