Canonical Allele Identifier: CA2695205875

Gene: NSD1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177235868_177235872delinsGATC , CM000667.2:g.177235868_177235872delinsGATC	GRCh38
NC_000005.9:g.176662869_176662873delinsGATC , CM000667.1:g.176662869_176662873delinsGATC	GRCh37
NC_000005.8:g.176595475_176595479delinsGATC	NCBI36
NG_009821.1:g.107790_107794delinsGATC , LRG_512:g.107790_107794delinsGATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508896.7:c.2971_2975delinsGATC	ENSP00000423372.3:p.Leu991AspfsTer27
ENST00000347982.9:c.2971_2975delinsGATC	ENSP00000343209.5:p.Leu991AspfsTer27
ENST00000354179.9:c.2971_2975delinsGATC	ENSP00000346111.5:p.Leu991AspfsTer27
ENST00000510954.6:n.660_664delinsGATC
ENST00000685206.1:n.3427_3431delinsGATC
ENST00000686993.1:c.2971_2975delinsGATC	ENSP00000510020.1:p.Leu991AspfsTer27
ENST00000687453.1:c.3535_3539delinsGATC	ENSP00000508426.1:p.Leu1179AspfsTer27
ENST00000688613.1:n.3241_3245delinsGATC
ENST00000689326.1:c.3844_3848delinsGATC	ENSP00000509594.1:p.Leu1282AspfsTer29
ENST00000689345.1:c.2971_2975delinsGATC	ENSP00000509711.1:p.Leu991AspfsTer27
ENST00000689549.1:n.3991_3995delinsGATC
ENST00000439151.7:c.3844_3848delinsGATC MANE Select	ENSP00000395929.2:p.Leu1282AspfsTer27
ENST00000347982.8:c.3037_3041delinsGATC	ENSP00000343209.4:p.Leu1013AspfsTer27
ENST00000354179.8:c.3037_3041delinsGATC	ENSP00000346111.4:p.Leu1013AspfsTer27
ENST00000375350.3:c.255_259delinsGATC	ENSP00000364499.3:n.255_259delinsGATC
ENST00000439151.6:c.3844_3848delinsGATC	ENSP00000395929.2:p.Leu1282AspfsTer27
NM_022455.4:c.3844_3848delinsGATC , LRG_512t1:c.3844_3848delinsGATC	NP_071900.2:p.Leu1282AspfsTer27
NM_172349.2:c.3037_3041delinsGATC	NP_758859.1:p.Leu1013AspfsTer27
XM_005265959.1:c.3844_3848delinsGATC	XP_005266016.1:p.Leu1282AspfsTer27
XM_005265960.1:c.3037_3041delinsGATC	XP_005266017.1:p.Leu1013AspfsTer27
XM_005265961.1:c.3037_3041delinsGATC	XP_005266018.1:p.Leu1013AspfsTer27
XM_011534610.1:c.3844_3848delinsGATC	XP_011532912.1:p.Leu1282AspfsTer27
XM_011534611.1:c.3844_3848delinsGATC	XP_011532913.1:p.Leu1282AspfsTer27
XM_011534612.1:c.3424_3428delinsGATC	XP_011532914.1:p.Leu1142AspfsTer27
XM_011534613.1:c.2788_2792delinsGATC	XP_011532915.1:p.Leu930AspfsTer27
XM_011534614.1:c.3844_3848delinsGATC	XP_011532916.1:p.Leu1282AspfsTer27
XM_011534615.1:c.3844_3848delinsGATC	XP_011532917.1:p.Leu1282AspfsTer27
XM_011534616.1:c.3844_3848delinsGATC	XP_011532918.1:p.Leu1282AspfsTer29
XM_011534617.1:c.-152_-148delinsGATC	XP_011532919.1:n.-152_-148delinsGATC
NM_001365684.1:c.3037_3041delinsGATC	NP_001352613.1:p.Leu1013AspfsTer27
XM_024446150.1:c.3844_3848delinsGATC	XP_024301918.1:p.Leu1282AspfsTer27
XM_024446151.1:c.3844_3848delinsGATC	XP_024301919.1:p.Leu1282AspfsTer27
XM_024446152.1:c.3844_3848delinsGATC	XP_024301920.1:p.Leu1282AspfsTer27
XM_024446153.1:c.3844_3848delinsGATC	XP_024301921.1:p.Leu1282AspfsTer27
XM_024446154.1:c.3424_3428delinsGATC	XP_024301922.1:p.Leu1142AspfsTer27
XM_024446155.1:c.3037_3041delinsGATC	XP_024301923.1:p.Leu1013AspfsTer27
XM_024446156.1:c.3037_3041delinsGATC	XP_024301924.1:p.Leu1013AspfsTer27
XM_024446158.1:c.3037_3041delinsGATC	XP_024301926.1:p.Leu1013AspfsTer27
XM_024446159.1:c.2788_2792delinsGATC	XP_024301927.1:p.Leu930AspfsTer27
XM_024446160.1:c.3844_3848delinsGATC	XP_024301928.1:p.Leu1282AspfsTer27
XM_024446161.1:c.3844_3848delinsGATC	XP_024301929.1:p.Leu1282AspfsTer27
XM_024446162.1:c.-152_-148delinsGATC	XP_024301930.1:n.-152_-148delinsGATC
NM_022455.5:c.3844_3848delinsGATC MANE Select	NP_071900.2:p.Leu1282AspfsTer27
NM_172349.3:c.3037_3041delinsGATC	NP_758859.1:p.Leu1013AspfsTer27