Canonical Allele Identifier: CA447960391

Gene: NSD1

Linked Data

• MyVariant Identifiers: chr5:g.176636954T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177209953T>C , CM000667.2:g.177209953T>C	GRCh38
NC_000005.9:g.176636954T>C , CM000667.1:g.176636954T>C	GRCh37
NC_000005.8:g.176569560T>C	NCBI36
NG_009821.1:g.81875T>C , LRG_512:g.81875T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000508896.7:c.681T>C	ENSP00000423372.3:p.Phe227=
ENST00000347982.9:c.681T>C	ENSP00000343209.5:p.Phe227=
ENST00000354179.9:c.681T>C	ENSP00000346111.5:p.Phe227=
ENST00000508896.6:c.681T>C	ENSP00000423372.2:p.Phe227=
ENST00000510954.6:n.612+5661T>C
ENST00000638627.3:c.498T>C	ENSP00000492679.3:p.Phe166=
ENST00000644863.2:c.498T>C	ENSP00000496157.2:p.Phe166=
ENST00000685206.1:n.1137T>C
ENST00000686993.1:c.681T>C	ENSP00000510020.1:p.Phe227=
ENST00000687453.1:c.1245T>C	ENSP00000508426.1:p.Phe415=
ENST00000688613.1:n.951T>C
ENST00000689326.1:c.1554T>C	ENSP00000509594.1:p.Phe518=
ENST00000689345.1:c.681T>C	ENSP00000509711.1:p.Phe227=
ENST00000689549.1:n.1701T>C
ENST00000439151.7:c.1554T>C MANE Select	ENSP00000395929.2:p.Phe518=
ENST00000638627.2:c.*647T>C	ENSP00000492679.2:n.*647T>C
ENST00000644863.1:c.*863T>C	ENSP00000496157.1:n.*863T>C
ENST00000347982.8:c.747T>C	ENSP00000343209.4:p.Phe249=
ENST00000354179.8:c.747T>C	ENSP00000346111.4:p.Phe249=
ENST00000439151.6:c.1554T>C	ENSP00000395929.2:p.Phe518=
NM_022455.4:c.1554T>C , LRG_512t1:c.1554T>C	NP_071900.2:p.Phe518=
NM_172349.2:c.747T>C	NP_758859.1:p.Phe249=
XM_005265959.1:c.1554T>C	XP_005266016.1:p.Phe518=
XM_005265960.1:c.747T>C	XP_005266017.1:p.Phe249=
XM_005265961.1:c.747T>C	XP_005266018.1:p.Phe249=
XM_011534610.1:c.1554T>C	XP_011532912.1:p.Phe518=
XM_011534611.1:c.1554T>C	XP_011532913.1:p.Phe518=
XM_011534612.1:c.1134T>C	XP_011532914.1:p.Phe378=
XM_011534613.1:c.498T>C	XP_011532915.1:p.Phe166=
XM_011534614.1:c.1554T>C	XP_011532916.1:p.Phe518=
XM_011534615.1:c.1554T>C	XP_011532917.1:p.Phe518=
XM_011534616.1:c.1554T>C	XP_011532918.1:p.Phe518=
NM_001365684.1:c.747T>C	NP_001352613.1:p.Phe249=
XM_024446150.1:c.1554T>C	XP_024301918.1:p.Phe518=
XM_024446151.1:c.1554T>C	XP_024301919.1:p.Phe518=
XM_024446152.1:c.1554T>C	XP_024301920.1:p.Phe518=
XM_024446153.1:c.1554T>C	XP_024301921.1:p.Phe518=
XM_024446154.1:c.1134T>C	XP_024301922.1:p.Phe378=
XM_024446155.1:c.747T>C	XP_024301923.1:p.Phe249=
XM_024446156.1:c.747T>C	XP_024301924.1:p.Phe249=
XM_024446158.1:c.747T>C	XP_024301926.1:p.Phe249=
XM_024446159.1:c.498T>C	XP_024301927.1:p.Phe166=
XM_024446160.1:c.1554T>C	XP_024301928.1:p.Phe518=
XM_024446161.1:c.1554T>C	XP_024301929.1:p.Phe518=
XM_024446162.1:c.-2442T>C	XP_024301930.1:n.-2442T>C
NM_022455.5:c.1554T>C MANE Select	NP_071900.2:p.Phe518=
NM_172349.3:c.747T>C	NP_758859.1:p.Phe249=