Canonical Allele Identifier: CA6665620

Gene: DPY19L2

Linked Data

• dbSNP Id: rs757564639
• ExAC: 12:64017808 A / C
• gnomAD v2: 12-64017808-A-C
• gnomAD v4: 12-63624028-A-C
• MyVariant Identifiers: chr12:g.64017808A>C (hg19) ; chr12:g.63624028A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.63624028A>C , CM000674.2:g.63624028A>C	GRCh38
NC_000012.11:g.64017808A>C , CM000674.1:g.64017808A>C	GRCh37
NC_000012.10:g.62304075A>C	NCBI36
NG_031909.1:g.49547T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000324472.9:c.953+12T>G MANE Select	ENSP00000315988.4:n.953+12T>G
ENST00000306389.7:c.*344+2441T>G	ENSP00000445878.1:n.*344+2441T>G
ENST00000324472.8:c.953+12T>G	ENSP00000315988.4:n.953+12T>G
NM_173812.4:c.953+12T>G	NP_776173.3:n.953+12T>G
XM_006719348.2:c.953+12T>G	XP_006719411.1:n.953+12T>G
XM_006719350.2:c.953+12T>G	XP_006719413.1:n.953+12T>G
XM_006719352.1:c.524+12T>G	XP_006719415.1:n.524+12T>G
XM_006719353.2:c.524+12T>G	XP_006719416.1:n.524+12T>G
XM_006719355.2:c.953+12T>G	XP_006719418.1:n.953+12T>G
XM_006719356.2:c.8+2441T>G	XP_006719419.1:n.8+2441T>G
XM_011538215.1:c.440+12T>G	XP_011536517.1:n.440+12T>G
XM_011538216.1:c.953+12T>G	XP_011536518.1:n.953+12T>G
XM_011538217.1:c.953+12T>G	XP_011536519.1:n.953+12T>G
XR_429092.2:n.1169+12T>G
XR_944521.1:n.1169+12T>G
XM_006719352.2:c.524+12T>G	XP_006719415.1:n.524+12T>G
XM_011538215.2:c.440+12T>G	XP_011536517.1:n.440+12T>G
XM_017019192.2:c.804-2691T>G	XP_016874681.1:n.804-2691T>G
XM_017019193.2:c.650+12T>G	XP_016874682.1:n.650+12T>G
XM_017019201.1:c.8+2441T>G	XP_016874690.1:n.8+2441T>G
XM_017019203.2:c.8+2441T>G	XP_016874692.1:n.8+2441T>G
XM_017019204.1:c.8+2441T>G	XP_016874693.1:n.8+2441T>G
XM_024448944.1:c.953+12T>G	XP_024304712.1:n.953+12T>G
XM_024448945.1:c.953+12T>G	XP_024304713.1:n.953+12T>G
XM_024448946.1:c.524+12T>G	XP_024304714.1:n.524+12T>G
XM_024448947.1:c.524+12T>G	XP_024304715.1:n.524+12T>G
XM_024448948.1:c.953+12T>G	XP_024304716.1:n.953+12T>G
XM_024448949.1:c.953+12T>G	XP_024304717.1:n.953+12T>G
XM_024448950.1:c.953+12T>G	XP_024304718.1:n.953+12T>G
XM_024448951.1:c.953+12T>G	XP_024304719.1:n.953+12T>G
XM_024448952.1:c.953+12T>G	XP_024304720.1:n.953+12T>G
XM_024448953.1:c.953+12T>G	XP_024304721.1:n.953+12T>G
XM_024448954.1:c.953+12T>G	XP_024304722.1:n.953+12T>G
XM_024448955.1:c.953+12T>G	XP_024304723.1:n.953+12T>G
XM_024448956.1:c.524+12T>G	XP_024304724.1:n.524+12T>G
XM_024448957.1:c.953+12T>G	XP_024304725.1:n.953+12T>G
XR_001748666.2:n.1105+12T>G
XR_002957314.1:n.1105+12T>G
XR_002957315.1:n.1105+12T>G
XR_002957316.1:n.1105+12T>G
XR_002957317.1:n.1105+12T>G
XR_002957318.1:n.1105+12T>G
XR_002957319.1:n.1105+12T>G
NM_173812.5:c.953+12T>G MANE Select	NP_776173.3:n.953+12T>G