Canonical Allele Identifier: CA2678464165

Gene: CDKN1A DINOL

Linked Data

• gnomAD v4: 6-36677928-G-T

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000448526.6:c.-11G>T (CDKN1A)	ENSP00000409259.3:n.-11G>T
ENST00000459970.1:n.184G>T (CDKN1A)
ENST00000615513.4:c.-6+1404G>T (CDKN1A)	ENSP00000482768.1:n.-6+1404G>T
NM_001220777.1:c.-6+1404G>T (CDKN1A)	NP_001207706.1:n.-6+1404G>T
NM_001291549.1:c.92G>T (CDKN1A)	NP_001278478.1:p.Cys31Phe
NM_078467.2:c.-11G>T (CDKN1A)	NP_510867.1:n.-11G>T
NR_144384.1:n.632C>A (DINOL)
NM_001220777.2:c.-6+1404G>T (CDKN1A)	NP_001207706.1:n.-6+1404G>T
NM_001291549.3:c.92G>T (CDKN1A)	NP_001278478.1:p.Cys31Phe
NM_001374509.1:c.92G>T (CDKN1A)	NP_001361438.1:p.Cys31Phe
NM_001374510.1:c.34+1358G>T (CDKN1A)	NP_001361439.1:n.34+1358G>T
NM_078467.3:c.-11G>T (CDKN1A)	NP_510867.1:n.-11G>T