Canonical Allele Identifier: CA2678464166

Gene: CDKN1A DINOL

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.36677928G>C , CM000668.2:g.36677928G>C	GRCh38
NC_000006.11:g.36645705G>C , CM000668.1:g.36645705G>C	GRCh37
NC_000006.10:g.36753683G>C	NCBI36
NG_009364.1:g.4247G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448526.6:c.-11G>C (CDKN1A)	ENSP00000409259.3:n.-11G>C
ENST00000459970.1:n.184G>C (CDKN1A)
ENST00000615513.4:c.-6+1404G>C (CDKN1A)	ENSP00000482768.1:n.-6+1404G>C
NM_001220777.1:c.-6+1404G>C (CDKN1A)	NP_001207706.1:n.-6+1404G>C
NM_001291549.1:c.92G>C (CDKN1A)	NP_001278478.1:p.Cys31Ser
NM_078467.2:c.-11G>C (CDKN1A)	NP_510867.1:n.-11G>C
NR_144384.1:n.632C>G (DINOL)
NM_001220777.2:c.-6+1404G>C (CDKN1A)	NP_001207706.1:n.-6+1404G>C
NM_001291549.3:c.92G>C (CDKN1A)	NP_001278478.1:p.Cys31Ser
NM_001374509.1:c.92G>C (CDKN1A)	NP_001361438.1:p.Cys31Ser
NM_001374510.1:c.34+1358G>C (CDKN1A)	NP_001361439.1:n.34+1358G>C
NM_078467.3:c.-11G>C (CDKN1A)	NP_510867.1:n.-11G>C