Canonical Allele Identifier: CA2041768191

Gene: DPY19L2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.63624148_63624149delinsGC , CM000674.2:g.63624148_63624149delinsGC	GRCh38
NC_000012.11:g.64017928_64017929delinsGC , CM000674.1:g.64017928_64017929delinsGC	GRCh37
NC_000012.10:g.62304195_62304196delinsGC	NCBI36
NG_031909.1:g.49426_49427delinsGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000324472.9:c.862-18_862-17delinsGC MANE Select	ENSP00000315988.4:n.862-18_862-17delinsGC
ENST00000306389.7:c.*344+2320_*344+2321delinsGC	ENSP00000445878.1:n.*344+2320_*344+2321delinsGC
ENST00000324472.8:c.862-18_862-17delinsGC	ENSP00000315988.4:n.862-18_862-17delinsGC
NM_173812.4:c.862-18_862-17delinsGC	NP_776173.3:n.862-18_862-17delinsGC
XM_006719348.2:c.862-18_862-17delinsGC	XP_006719411.1:n.862-18_862-17delinsGC
XM_006719350.2:c.862-18_862-17delinsGC	XP_006719413.1:n.862-18_862-17delinsGC
XM_006719352.1:c.433-18_433-17delinsGC	XP_006719415.1:n.433-18_433-17delinsGC
XM_006719353.2:c.433-18_433-17delinsGC	XP_006719416.1:n.433-18_433-17delinsGC
XM_006719355.2:c.862-18_862-17delinsGC	XP_006719418.1:n.862-18_862-17delinsGC
XM_006719356.2:c.8+2320_8+2321delinsGC	XP_006719419.1:n.8+2320_8+2321delinsGC
XM_011538215.1:c.349-18_349-17delinsGC	XP_011536517.1:n.349-18_349-17delinsGC
XM_011538216.1:c.862-18_862-17delinsGC	XP_011536518.1:n.862-18_862-17delinsGC
XM_011538217.1:c.862-18_862-17delinsGC	XP_011536519.1:n.862-18_862-17delinsGC
XR_429092.2:n.1078-18_1078-17delinsGC
XR_944521.1:n.1078-18_1078-17delinsGC
XM_006719352.2:c.433-18_433-17delinsGC	XP_006719415.1:n.433-18_433-17delinsGC
XM_011538215.2:c.349-18_349-17delinsGC	XP_011536517.1:n.349-18_349-17delinsGC
XM_017019192.2:c.804-2812_804-2811delinsGC	XP_016874681.1:n.804-2812_804-2811delinsGC
XM_017019193.2:c.559-18_559-17delinsGC	XP_016874682.1:n.559-18_559-17delinsGC
XM_017019201.1:c.8+2320_8+2321delinsGC	XP_016874690.1:n.8+2320_8+2321delinsGC
XM_017019203.2:c.8+2320_8+2321delinsGC	XP_016874692.1:n.8+2320_8+2321delinsGC
XM_017019204.1:c.8+2320_8+2321delinsGC	XP_016874693.1:n.8+2320_8+2321delinsGC
XM_024448944.1:c.862-18_862-17delinsGC	XP_024304712.1:n.862-18_862-17delinsGC
XM_024448945.1:c.862-18_862-17delinsGC	XP_024304713.1:n.862-18_862-17delinsGC
XM_024448946.1:c.433-18_433-17delinsGC	XP_024304714.1:n.433-18_433-17delinsGC
XM_024448947.1:c.433-18_433-17delinsGC	XP_024304715.1:n.433-18_433-17delinsGC
XM_024448948.1:c.862-18_862-17delinsGC	XP_024304716.1:n.862-18_862-17delinsGC
XM_024448949.1:c.862-18_862-17delinsGC	XP_024304717.1:n.862-18_862-17delinsGC
XM_024448950.1:c.862-18_862-17delinsGC	XP_024304718.1:n.862-18_862-17delinsGC
XM_024448951.1:c.862-18_862-17delinsGC	XP_024304719.1:n.862-18_862-17delinsGC
XM_024448952.1:c.862-18_862-17delinsGC	XP_024304720.1:n.862-18_862-17delinsGC
XM_024448953.1:c.862-18_862-17delinsGC	XP_024304721.1:n.862-18_862-17delinsGC
XM_024448954.1:c.862-18_862-17delinsGC	XP_024304722.1:n.862-18_862-17delinsGC
XM_024448955.1:c.862-18_862-17delinsGC	XP_024304723.1:n.862-18_862-17delinsGC
XM_024448956.1:c.433-18_433-17delinsGC	XP_024304724.1:n.433-18_433-17delinsGC
XM_024448957.1:c.862-18_862-17delinsGC	XP_024304725.1:n.862-18_862-17delinsGC
XR_001748666.2:n.1014-18_1014-17delinsGC
XR_002957314.1:n.1014-18_1014-17delinsGC
XR_002957315.1:n.1014-18_1014-17delinsGC
XR_002957316.1:n.1014-18_1014-17delinsGC
XR_002957317.1:n.1014-18_1014-17delinsGC
XR_002957318.1:n.1014-18_1014-17delinsGC
XR_002957319.1:n.1014-18_1014-17delinsGC
NM_173812.5:c.862-18_862-17delinsGC MANE Select	NP_776173.3:n.862-18_862-17delinsGC