Canonical Allele Identifier: CA467832598

Gene: NOTCH1

Linked Data

• MyVariant Identifiers: chr9:g.139391789G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136497337G>C , CM000671.2:g.136497337G>C	GRCh38
NC_000009.11:g.139391789G>C , CM000671.1:g.139391789G>C	GRCh37
NC_000009.10:g.138511610G>C	NCBI36
NG_007458.1:g.53450C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651671.1:c.6402C>G MANE Select	ENSP00000498587.1:p.Thr2134=
ENST00000679595.1:c.*1442C>G	ENSP00000506241.1:n.*1442C>G
ENST00000679969.1:n.2998C>G
ENST00000680003.1:n.2734C>G
ENST00000680133.1:c.6288C>G	ENSP00000505319.1:p.Thr2096=
ENST00000680218.1:c.6282C>G	ENSP00000505339.1:p.Thr2094=
ENST00000680668.1:c.6288C>G	ENSP00000506336.1:p.Thr2096=
ENST00000680778.1:c.3999C>G	ENSP00000506033.1:p.Thr1333=
ENST00000680924.1:c.*3802C>G	ENSP00000506031.1:n.*3802C>G
ENST00000681135.1:c.*4011C>G	ENSP00000506636.1:n.*4011C>G
ENST00000681298.1:n.4507C>G
ENST00000681454.1:c.*5638C>G	ENSP00000505763.1:n.*5638C>G
ENST00000277541.6:c.6402C>G	ENSP00000277541.6:p.Thr2134=
NM_017617.3:c.6402C>G	NP_060087.3:p.Thr2134=
XM_011518717.1:c.5703C>G	XP_011517019.1:p.Thr1901=
NM_017617.5:c.6402C>G MANE Select	NP_060087.3:p.Thr2134=
XM_011518717.2:c.5679C>G	XP_011517019.2:p.Thr1893=