Canonical Allele Identifier: CA2578494963

Gene: NSD1

Linked Data

• gnomAD v4: 5-177260185-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177260185_177260186insA , CM000667.2:g.177260185_177260186insA	GRCh38
NC_000005.9:g.176687186_176687187insA , CM000667.1:g.176687186_176687187insA	GRCh37
NC_000005.8:g.176619792_176619793insA	NCBI36
NG_009821.1:g.132107_132108insA , LRG_512:g.132107_132108insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508896.7:c.4273+17_4273+18insA	ENSP00000423372.3:n.4273+17_4273+18insA
ENST00000347982.9:c.4273+17_4273+18insA	ENSP00000343209.5:n.4273+17_4273+18insA
ENST00000354179.9:c.4273+17_4273+18insA	ENSP00000346111.5:n.4273+17_4273+18insA
ENST00000685206.1:n.4729+17_4729+18insA
ENST00000686993.1:c.4273+17_4273+18insA	ENSP00000510020.1:n.4273+17_4273+18insA
ENST00000687453.1:c.4837+17_4837+18insA	ENSP00000508426.1:n.4837+17_4837+18insA
ENST00000688613.1:n.4543+17_4543+18insA
ENST00000689345.1:c.4273+17_4273+18insA	ENSP00000509711.1:n.4273+17_4273+18insA
ENST00000689549.1:n.5293+17_5293+18insA
ENST00000439151.7:c.5146+17_5146+18insA MANE Select	ENSP00000395929.2:n.5146+17_5146+18insA
ENST00000347982.8:c.4339+17_4339+18insA	ENSP00000343209.4:n.4339+17_4339+18insA
ENST00000354179.8:c.4339+17_4339+18insA	ENSP00000346111.4:n.4339+17_4339+18insA
ENST00000439151.6:c.5146+17_5146+18insA	ENSP00000395929.2:n.5146+17_5146+18insA
NM_022455.4:c.5146+17_5146+18insA , LRG_512t1:c.5146+17_5146+18insA	NP_071900.2:n.5146+17_5146+18insA
NM_172349.2:c.4339+17_4339+18insA	NP_758859.1:n.4339+17_4339+18insA
XM_005265959.1:c.5146+17_5146+18insA	XP_005266016.1:n.5146+17_5146+18insA
XM_005265960.1:c.4339+17_4339+18insA	XP_005266017.1:n.4339+17_4339+18insA
XM_005265961.1:c.4339+17_4339+18insA	XP_005266018.1:n.4339+17_4339+18insA
XM_005265962.3:c.640+17_640+18insA	XP_005266019.1:n.640+17_640+18insA
XM_011534610.1:c.5146+17_5146+18insA	XP_011532912.1:n.5146+17_5146+18insA
XM_011534611.1:c.5146+17_5146+18insA	XP_011532913.1:n.5146+17_5146+18insA
XM_011534612.1:c.4726+17_4726+18insA	XP_011532914.1:n.4726+17_4726+18insA
XM_011534613.1:c.4090+17_4090+18insA	XP_011532915.1:n.4090+17_4090+18insA
XM_011534614.1:c.5146+17_5146+18insA	XP_011532916.1:n.5146+17_5146+18insA
XM_011534617.1:c.880+17_880+18insA	XP_011532919.1:n.880+17_880+18insA
NM_001365684.1:c.4339+17_4339+18insA	NP_001352613.1:n.4339+17_4339+18insA
XM_024446150.1:c.5146+17_5146+18insA	XP_024301918.1:n.5146+17_5146+18insA
XM_024446151.1:c.5146+17_5146+18insA	XP_024301919.1:n.5146+17_5146+18insA
XM_024446152.1:c.5146+17_5146+18insA	XP_024301920.1:n.5146+17_5146+18insA
XM_024446153.1:c.5146+17_5146+18insA	XP_024301921.1:n.5146+17_5146+18insA
XM_024446154.1:c.4726+17_4726+18insA	XP_024301922.1:n.4726+17_4726+18insA
XM_024446155.1:c.4339+17_4339+18insA	XP_024301923.1:n.4339+17_4339+18insA
XM_024446156.1:c.4339+17_4339+18insA	XP_024301924.1:n.4339+17_4339+18insA
XM_024446158.1:c.4339+17_4339+18insA	XP_024301926.1:n.4339+17_4339+18insA
XM_024446159.1:c.4090+17_4090+18insA	XP_024301927.1:n.4090+17_4090+18insA
XM_024446160.1:c.5146+17_5146+18insA	XP_024301928.1:n.5146+17_5146+18insA
XM_024446162.1:c.880+17_880+18insA	XP_024301930.1:n.880+17_880+18insA
XM_024446163.1:c.640+17_640+18insA	XP_024301931.1:n.640+17_640+18insA
NM_022455.5:c.5146+17_5146+18insA MANE Select	NP_071900.2:n.5146+17_5146+18insA
NM_172349.3:c.4339+17_4339+18insA	NP_758859.1:n.4339+17_4339+18insA