Canonical Allele Identifier: CA467832221

Gene: NOTCH1

Linked Data

• MyVariant Identifiers: chr9:g.139391618C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136497166C>G , CM000671.2:g.136497166C>G	GRCh38
NC_000009.11:g.139391618C>G , CM000671.1:g.139391618C>G	GRCh37
NC_000009.10:g.138511439C>G	NCBI36
NG_007458.1:g.53621G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651671.1:c.6573G>C MANE Select	ENSP00000498587.1:p.Leu2191=
ENST00000679595.1:c.*1613G>C	ENSP00000506241.1:n.*1613G>C
ENST00000679969.1:n.3169G>C
ENST00000680003.1:n.2905G>C
ENST00000680133.1:c.6459G>C	ENSP00000505319.1:p.Leu2153=
ENST00000680218.1:c.6453G>C	ENSP00000505339.1:p.Leu2151=
ENST00000680668.1:c.6459G>C	ENSP00000506336.1:p.Leu2153=
ENST00000680778.1:c.4170G>C	ENSP00000506033.1:p.Leu1390=
ENST00000680924.1:c.*3973G>C	ENSP00000506031.1:n.*3973G>C
ENST00000681135.1:c.*4182G>C	ENSP00000506636.1:n.*4182G>C
ENST00000681298.1:n.4678G>C
ENST00000681454.1:c.*5809G>C	ENSP00000505763.1:n.*5809G>C
ENST00000277541.6:c.6573G>C	ENSP00000277541.6:p.Leu2191=
NM_017617.3:c.6573G>C	NP_060087.3:p.Leu2191=
XM_011518717.1:c.5874G>C	XP_011517019.1:p.Leu1958=
NM_017617.5:c.6573G>C MANE Select	NP_060087.3:p.Leu2191=
XM_011518717.2:c.5850G>C	XP_011517019.2:p.Leu1950=