Canonical Allele Identifier: CA1603475958

Gene: NSD1

Linked Data

• ClinVar Variation Id: 1036621
• ClinVar RCV Id: RCV003232316
• dbSNP Id: rs1763273634

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177210751_177210752delinsAA , CM000667.2:g.177210751_177210752delinsAA	GRCh38
NC_000005.9:g.176637752_176637753delinsAA , CM000667.1:g.176637752_176637753delinsAA	GRCh37
NC_000005.8:g.176570358_176570359delinsAA	NCBI36
NG_009821.1:g.82673_82674delinsAA , LRG_512:g.82673_82674delinsAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508896.7:c.1479_1480delinsAA	ENSP00000423372.3:p.Pro494Thr
ENST00000347982.9:c.1479_1480delinsAA	ENSP00000343209.5:p.Pro494Thr
ENST00000354179.9:c.1479_1480delinsAA	ENSP00000346111.5:p.Pro494Thr
ENST00000510954.6:n.612+6459_612+6460delinsAA
ENST00000685206.1:n.1935_1936delinsAA
ENST00000686993.1:c.1479_1480delinsAA	ENSP00000510020.1:p.Pro494Thr
ENST00000687453.1:c.2043_2044delinsAA	ENSP00000508426.1:p.Pro682Thr
ENST00000688613.1:n.1749_1750delinsAA
ENST00000689326.1:c.2352_2353delinsAA	ENSP00000509594.1:p.Pro785Thr
ENST00000689345.1:c.1479_1480delinsAA	ENSP00000509711.1:p.Pro494Thr
ENST00000689549.1:n.2499_2500delinsAA
ENST00000439151.7:c.2352_2353delinsAA MANE Select	ENSP00000395929.2:p.Pro785Thr
ENST00000347982.8:c.1545_1546delinsAA	ENSP00000343209.4:p.Pro516Thr
ENST00000354179.8:c.1545_1546delinsAA	ENSP00000346111.4:p.Pro516Thr
ENST00000439151.6:c.2352_2353delinsAA	ENSP00000395929.2:p.Pro785Thr
NM_022455.4:c.2352_2353delinsAA , LRG_512t1:c.2352_2353delinsAA	NP_071900.2:p.Pro785Thr
NM_172349.2:c.1545_1546delinsAA	NP_758859.1:p.Pro516Thr
XM_005265959.1:c.2352_2353delinsAA	XP_005266016.1:p.Pro785Thr
XM_005265960.1:c.1545_1546delinsAA	XP_005266017.1:p.Pro516Thr
XM_005265961.1:c.1545_1546delinsAA	XP_005266018.1:p.Pro516Thr
XM_011534610.1:c.2352_2353delinsAA	XP_011532912.1:p.Pro785Thr
XM_011534611.1:c.2352_2353delinsAA	XP_011532913.1:p.Pro785Thr
XM_011534612.1:c.1932_1933delinsAA	XP_011532914.1:p.Pro645Thr
XM_011534613.1:c.1296_1297delinsAA	XP_011532915.1:p.Pro433Thr
XM_011534614.1:c.2352_2353delinsAA	XP_011532916.1:p.Pro785Thr
XM_011534615.1:c.2352_2353delinsAA	XP_011532917.1:p.Pro785Thr
XM_011534616.1:c.2352_2353delinsAA	XP_011532918.1:p.Pro785Thr
NM_001365684.1:c.1545_1546delinsAA	NP_001352613.1:p.Pro516Thr
XM_024446150.1:c.2352_2353delinsAA	XP_024301918.1:p.Pro785Thr
XM_024446151.1:c.2352_2353delinsAA	XP_024301919.1:p.Pro785Thr
XM_024446152.1:c.2352_2353delinsAA	XP_024301920.1:p.Pro785Thr
XM_024446153.1:c.2352_2353delinsAA	XP_024301921.1:p.Pro785Thr
XM_024446154.1:c.1932_1933delinsAA	XP_024301922.1:p.Pro645Thr
XM_024446155.1:c.1545_1546delinsAA	XP_024301923.1:p.Pro516Thr
XM_024446156.1:c.1545_1546delinsAA	XP_024301924.1:p.Pro516Thr
XM_024446158.1:c.1545_1546delinsAA	XP_024301926.1:p.Pro516Thr
XM_024446159.1:c.1296_1297delinsAA	XP_024301927.1:p.Pro433Thr
XM_024446160.1:c.2352_2353delinsAA	XP_024301928.1:p.Pro785Thr
XM_024446161.1:c.2352_2353delinsAA	XP_024301929.1:p.Pro785Thr
XM_024446162.1:c.-1644_-1643delinsAA	XP_024301930.1:n.-1644_-1643delinsAA
NM_022455.5:c.2352_2353delinsAA MANE Select	NP_071900.2:p.Pro785Thr
NM_172349.3:c.1545_1546delinsAA	NP_758859.1:p.Pro516Thr