Canonical Allele Identifier: CA137419052

Gene: CDKN1A

Linked Data

• dbSNP Id: rs1017678166
• gnomAD v2: 6-36648900-G-A
• gnomAD v3: 6-36681123-G-A
• gnomAD v4: 6-36681123-G-A
• MyVariant Identifiers: chr6:g.36648900G>A (hg19) ; chr6:g.36681123G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.36681123G>A , CM000668.2:g.36681123G>A	GRCh38
NC_000006.11:g.36648900G>A , CM000668.1:g.36648900G>A	GRCh37
NC_000006.10:g.36756878G>A	NCBI36
NG_009364.1:g.7442G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244741.10:c.-6+2325G>A MANE Select	ENSP00000244741.6:n.-6+2325G>A
ENST00000244741.9:c.-6+2325G>A	ENSP00000244741.5:n.-6+2325G>A
ENST00000373711.3:c.-96-1517G>A	ENSP00000362815.1:n.-96-1517G>A
ENST00000405375.5:c.-6+2184G>A	ENSP00000384849.1:n.-6+2184G>A
ENST00000448526.6:c.-5-2974G>A	ENSP00000409259.3:n.-5-2974G>A
ENST00000459970.1:n.190-2974G>A
ENST00000478800.1:n.214+2184G>A
ENST00000615513.4:c.-5-2974G>A	ENSP00000482768.1:n.-5-2974G>A
NM_000389.4:c.-6+2325G>A	NP_000380.1:n.-6+2325G>A
NM_001220777.1:c.-5-2974G>A	NP_001207706.1:n.-5-2974G>A
NM_001220778.1:c.-6+2184G>A	NP_001207707.1:n.-6+2184G>A
NM_001291549.1:c.98-2974G>A	NP_001278478.1:n.98-2974G>A
NM_078467.2:c.-5-2974G>A	NP_510867.1:n.-5-2974G>A
XM_011515041.1:c.*269G>A	XP_011513343.1:n.*269G>A
NM_000389.5:c.-6+2325G>A MANE Select	NP_000380.1:n.-6+2325G>A
NM_001220777.2:c.-5-2974G>A	NP_001207706.1:n.-5-2974G>A
NM_001220778.2:c.-6+2184G>A	NP_001207707.1:n.-6+2184G>A
NM_001291549.3:c.98-2974G>A	NP_001278478.1:n.98-2974G>A
NM_001374509.1:c.98-2974G>A	NP_001361438.1:n.98-2974G>A
NM_001374510.1:c.35-2974G>A	NP_001361439.1:n.35-2974G>A
NM_001374511.1:c.-6+2325G>A	NP_001361440.1:n.-6+2325G>A
NM_001374512.1:c.-6+2325G>A	NP_001361441.1:n.-6+2325G>A
NM_001374513.1:c.-6+2218G>A	NP_001361442.1:n.-6+2218G>A
NM_078467.3:c.-5-2974G>A	NP_510867.1:n.-5-2974G>A