Canonical Allele Identifier: CA410422731

Gene: DNMT3L

Linked Data

• gnomAD v4: 21-44261177-G-C
• MyVariant Identifiers: chr21:g.45681060G>C (hg19) ; chr21:g.44261177G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44261177G>C , CM000683.2:g.44261177G>C	GRCh38
NC_000021.8:g.45681060G>C , CM000683.1:g.45681060G>C	GRCh37
NC_000021.7:g.44505488G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000628202.3:c.83C>G MANE Select	ENSP00000486001.1:p.Ser28Cys
ENST00000270172.7:c.83C>G	ENSP00000270172.3:p.Ser28Cys
ENST00000431166.1:c.83C>G	ENSP00000400242.1:p.Ser28Cys
ENST00000628202.2:c.83C>G	ENSP00000486001.1:p.Ser28Cys
NM_013369.3:c.83C>G	NP_037501.2:p.Ser28Cys
NM_175867.2:c.83C>G	NP_787063.1:p.Ser28Cys
XM_011529536.1:c.83C>G	XP_011527838.1:p.Ser28Cys
NM_013369.4:c.83C>G	NP_037501.2:p.Ser28Cys
NM_175867.3:c.83C>G MANE Select	NP_787063.1:p.Ser28Cys