Canonical Allele Identifier: CA2618605500

Gene: KMT2D

Linked Data

• gnomAD v4: 12-49022404-AGTGGTGGCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49022409_49022417del , CM000674.2:g.49022409_49022417del	GRCh38
NC_000012.11:g.49416192_49416200del , CM000674.1:g.49416192_49416200del	GRCh37
NC_000012.10:g.47702459_47702467del	NCBI36
NG_027827.1:g.37912_37920del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526209.2:c.309-60_309-52del
ENST00000681974.1:n.1011-60_1011-52del
ENST00000682693.1:n.1973-60_1973-52del
ENST00000682886.1:n.685_693del
ENST00000683543.2:c.16387-60_16387-52del	ENSP00000506726.1:n.16387-60_16387-52del
ENST00000683988.1:c.310-60_310-52del	ENSP00000506939.1:n.310-60_310-52del
ENST00000684428.1:c.874-2_880del
ENST00000685024.1:c.1493-60_1493-52del
ENST00000685166.1:c.16348-60_16348-52del	ENSP00000509386.1:n.16348-60_16348-52del
ENST00000691932.1:c.340-60_340-52del	ENSP00000509037.1:n.340-60_340-52del
ENST00000692637.1:c.16336-60_16336-52del	ENSP00000509666.1:n.16336-60_16336-52del
ENST00000301067.12:c.16339-60_16339-52del MANE Select	ENSP00000301067.7:n.16339-60_16339-52del
ENST00000301067.11:c.16339-60_16339-52del	ENSP00000301067.7:n.16339-60_16339-52del
ENST00000526209.1:c.382-60_382-52del	ENSP00000435714.1:n.382-60_382-52del
NM_003482.3:c.16339-60_16339-52del	NP_003473.3:n.16339-60_16339-52del
XM_005269162.3:c.16339-60_16339-52del	XP_005269219.1:n.16339-60_16339-52del
XM_006719614.2:c.16348-60_16348-52del	XP_006719677.1:n.16348-60_16348-52del
XM_006719616.2:c.16336-60_16336-52del	XP_006719679.1:n.16336-60_16336-52del
XM_011538770.1:c.16396-60_16396-52del	XP_011537072.1:n.16396-60_16396-52del
XM_011538771.1:c.16393-60_16393-52del	XP_011537073.1:n.16393-60_16393-52del
XM_011538772.1:c.16387-60_16387-52del	XP_011537074.1:n.16387-60_16387-52del
XM_011538773.1:c.16384-60_16384-52del	XP_011537075.1:n.16384-60_16384-52del
XM_011538774.1:c.16375-60_16375-52del	XP_011537076.1:n.16375-60_16375-52del
XM_011538775.1:c.16330-60_16330-52del	XP_011537077.1:n.16330-60_16330-52del
XM_011538776.1:c.16303-60_16303-52del	XP_011537078.1:n.16303-60_16303-52del
XM_005269162.4:c.16339-60_16339-52del	XP_005269219.1:n.16339-60_16339-52del
XM_006719614.4:c.16348-60_16348-52del	XP_006719677.1:n.16348-60_16348-52del
XM_006719616.3:c.16336-60_16336-52del	XP_006719679.1:n.16336-60_16336-52del
XM_011538770.2:c.16396-60_16396-52del	XP_011537072.1:n.16396-60_16396-52del
XM_011538771.2:c.16393-60_16393-52del	XP_011537073.1:n.16393-60_16393-52del
XM_011538772.2:c.16387-60_16387-52del	XP_011537074.1:n.16387-60_16387-52del
XM_011538773.2:c.16384-60_16384-52del	XP_011537075.1:n.16384-60_16384-52del
XM_011538774.2:c.16375-60_16375-52del	XP_011537076.1:n.16375-60_16375-52del
XM_011538776.2:c.16303-60_16303-52del	XP_011537078.1:n.16303-60_16303-52del
XR_001748874.1:n.16516-60_16516-52del
NM_003482.4:c.16339-60_16339-52del MANE Select	NP_003473.3:n.16339-60_16339-52del