Canonical Allele Identifier: CA375631289

Gene: NOTCH1

Linked Data

• MyVariant Identifiers: chr9:g.139391638C>A (hg19) ; chr9:g.136497186C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136497186C>A , CM000671.2:g.136497186C>A	GRCh38
NC_000009.11:g.139391638C>A , CM000671.1:g.139391638C>A	GRCh37
NC_000009.10:g.138511459C>A	NCBI36
NG_007458.1:g.53601G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651671.1:c.6553G>T MANE Select	ENSP00000498587.1:p.Asp2185Tyr
ENST00000679595.1:c.*1593G>T	ENSP00000506241.1:n.*1593G>T
ENST00000679969.1:n.3149G>T
ENST00000680003.1:n.2885G>T
ENST00000680133.1:c.6439G>T	ENSP00000505319.1:p.Asp2147Tyr
ENST00000680218.1:c.6433G>T	ENSP00000505339.1:p.Asp2145Tyr
ENST00000680668.1:c.6439G>T	ENSP00000506336.1:p.Asp2147Tyr
ENST00000680778.1:c.4150G>T	ENSP00000506033.1:p.Asp1384Tyr
ENST00000680924.1:c.*3953G>T	ENSP00000506031.1:n.*3953G>T
ENST00000681135.1:c.*4162G>T	ENSP00000506636.1:n.*4162G>T
ENST00000681298.1:n.4658G>T
ENST00000681454.1:c.*5789G>T	ENSP00000505763.1:n.*5789G>T
ENST00000277541.6:c.6553G>T	ENSP00000277541.6:p.Asp2185Tyr
NM_017617.3:c.6553G>T	NP_060087.3:p.Asp2185Tyr
XM_011518717.1:c.5854G>T	XP_011517019.1:p.Asp1952Tyr
NM_017617.5:c.6553G>T MANE Select	NP_060087.3:p.Asp2185Tyr
XM_011518717.2:c.5830G>T	XP_011517019.2:p.Asp1944Tyr