Canonical Allele Identifier: CA2336659143

Gene: DMRTC2

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41850561C>G , CM000681.2:g.41850561C>G	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269945.8:c.852C>G MANE Select	ENSP00000269945.2:p.Gly284=
ENST00000269945.7:c.852C>G	ENSP00000269945.2:p.Gly284=
ENST00000596827.5:c.1005C>G	ENSP00000469525.1:p.Gly335=
ENST00000599022.1:n.318C>G
ENST00000601660.5:c.*370C>G	ENSP00000472159.1:n.*370C>G
NM_001040283.2:c.852C>G	NP_001035373.1:p.Gly284=
XM_005259146.3:c.861C>G	XP_005259203.1:p.Gly287=
XM_005259148.3:c.852C>G	XP_005259205.1:p.Gly284=
XM_011527212.1:c.852C>G	XP_011525514.1:p.Gly284=
XM_011527213.1:c.852C>G	XP_011525515.1:p.Gly284=
XM_011527214.1:c.483C>G	XP_011525516.1:p.Gly161=
XM_011527215.1:c.483C>G	XP_011525517.1:p.Gly161=
XM_017027123.1:c.1020C>G	XP_016882612.1:p.Gly340=
XM_017027124.2:c.1014C>G	XP_016882613.1:p.Gly338=
XM_017027125.1:c.1005C>G	XP_016882614.1:p.Gly335=
XM_017027126.2:c.1005C>G	XP_016882615.1:p.Gly335=
XM_017027127.2:c.1005C>G	XP_016882616.1:p.Gly335=
XM_017027128.1:c.1005C>G	XP_016882617.1:p.Gly335=
XM_017027129.1:c.867C>G	XP_016882618.1:p.Gly289=
NM_001040283.3:c.852C>G MANE Select	NP_001035373.1:p.Gly284=