Canonical Allele Identifier: CA1603529758

Gene: NSD1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177251818_177251820delinsCAA , CM000667.2:g.177251818_177251820delinsCAA	GRCh38
NC_000005.9:g.176678819_176678821delinsCAA , CM000667.1:g.176678819_176678821delinsCAA	GRCh37
NC_000005.8:g.176611425_176611427delinsCAA	NCBI36
NG_009821.1:g.123740_123742delinsCAA , LRG_512:g.123740_123742delinsCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508896.7:c.3857_3859delinsCAA	ENSP00000423372.3:p.Pro1286=
ENST00000347982.9:c.3857_3859delinsCAA	ENSP00000343209.5:p.Pro1286=
ENST00000354179.9:c.3857_3859delinsCAA	ENSP00000346111.5:p.Pro1286=
ENST00000685206.1:n.4313_4315delinsCAA
ENST00000686993.1:c.3857_3859delinsCAA	ENSP00000510020.1:p.Pro1286=
ENST00000687453.1:c.4421_4423delinsCAA	ENSP00000508426.1:p.Pro1474=
ENST00000688613.1:n.4127_4129delinsCAA
ENST00000689345.1:c.3857_3859delinsCAA	ENSP00000509711.1:p.Pro1286=
ENST00000689549.1:n.4877_4879delinsCAA
ENST00000439151.7:c.4730_4732delinsCAA MANE Select	ENSP00000395929.2:p.Pro1577=
ENST00000347982.8:c.3923_3925delinsCAA	ENSP00000343209.4:p.Pro1308=
ENST00000354179.8:c.3923_3925delinsCAA	ENSP00000346111.4:p.Pro1308=
ENST00000439151.6:c.4730_4732delinsCAA	ENSP00000395929.2:p.Pro1577=
NM_022455.4:c.4730_4732delinsCAA , LRG_512t1:c.4730_4732delinsCAA	NP_071900.2:p.Pro1577=
NM_172349.2:c.3923_3925delinsCAA	NP_758859.1:p.Pro1308=
XM_005265959.1:c.4730_4732delinsCAA	XP_005266016.1:p.Pro1577=
XM_005265960.1:c.3923_3925delinsCAA	XP_005266017.1:p.Pro1308=
XM_005265961.1:c.3923_3925delinsCAA	XP_005266018.1:p.Pro1308=
XM_005265962.3:c.224_226delinsCAA	XP_005266019.1:p.Pro75=
XM_011534610.1:c.4730_4732delinsCAA	XP_011532912.1:p.Pro1577=
XM_011534611.1:c.4730_4732delinsCAA	XP_011532913.1:p.Pro1577=
XM_011534612.1:c.4310_4312delinsCAA	XP_011532914.1:p.Pro1437=
XM_011534613.1:c.3674_3676delinsCAA	XP_011532915.1:p.Pro1225=
XM_011534614.1:c.4730_4732delinsCAA	XP_011532916.1:p.Pro1577=
XM_011534617.1:c.464_466delinsCAA	XP_011532919.1:p.Pro155=
NM_001365684.1:c.3923_3925delinsCAA	NP_001352613.1:p.Pro1308=
XM_024446150.1:c.4730_4732delinsCAA	XP_024301918.1:p.Pro1577=
XM_024446151.1:c.4730_4732delinsCAA	XP_024301919.1:p.Pro1577=
XM_024446152.1:c.4730_4732delinsCAA	XP_024301920.1:p.Pro1577=
XM_024446153.1:c.4730_4732delinsCAA	XP_024301921.1:p.Pro1577=
XM_024446154.1:c.4310_4312delinsCAA	XP_024301922.1:p.Pro1437=
XM_024446155.1:c.3923_3925delinsCAA	XP_024301923.1:p.Pro1308=
XM_024446156.1:c.3923_3925delinsCAA	XP_024301924.1:p.Pro1308=
XM_024446158.1:c.3923_3925delinsCAA	XP_024301926.1:p.Pro1308=
XM_024446159.1:c.3674_3676delinsCAA	XP_024301927.1:p.Pro1225=
XM_024446160.1:c.4730_4732delinsCAA	XP_024301928.1:p.Pro1577=
XM_024446162.1:c.464_466delinsCAA	XP_024301930.1:p.Pro155=
XM_024446163.1:c.224_226delinsCAA	XP_024301931.1:p.Pro75=
NM_022455.5:c.4730_4732delinsCAA MANE Select	NP_071900.2:p.Pro1577=
NM_172349.3:c.3923_3925delinsCAA	NP_758859.1:p.Pro1308=