Canonical Allele Identifier: CA375631930

Gene: NOTCH1

Linked Data

• gnomAD v4: 9-136497390-T-G
• MyVariant Identifiers: chr9:g.139391842T>G (hg19) ; chr9:g.136497390T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136497390T>G , CM000671.2:g.136497390T>G	GRCh38
NC_000009.11:g.139391842T>G , CM000671.1:g.139391842T>G	GRCh37
NC_000009.10:g.138511663T>G	NCBI36
NG_007458.1:g.53397A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651671.1:c.6349A>C MANE Select	ENSP00000498587.1:p.Asn2117His
ENST00000679595.1:c.*1389A>C	ENSP00000506241.1:n.*1389A>C
ENST00000679969.1:n.2945A>C
ENST00000680003.1:n.2681A>C
ENST00000680133.1:c.6235A>C	ENSP00000505319.1:p.Asn2079His
ENST00000680218.1:c.6229A>C	ENSP00000505339.1:p.Asn2077His
ENST00000680668.1:c.6235A>C	ENSP00000506336.1:p.Asn2079His
ENST00000680778.1:c.3946A>C	ENSP00000506033.1:p.Asn1316His
ENST00000680924.1:c.*3749A>C	ENSP00000506031.1:n.*3749A>C
ENST00000681135.1:c.*3958A>C	ENSP00000506636.1:n.*3958A>C
ENST00000681298.1:n.4454A>C
ENST00000681454.1:c.*5585A>C	ENSP00000505763.1:n.*5585A>C
ENST00000277541.6:c.6349A>C	ENSP00000277541.6:p.Asn2117His
NM_017617.3:c.6349A>C	NP_060087.3:p.Asn2117His
XM_011518717.1:c.5650A>C	XP_011517019.1:p.Asn1884His
NM_017617.5:c.6349A>C MANE Select	NP_060087.3:p.Asn2117His
XM_011518717.2:c.5626A>C	XP_011517019.2:p.Asn1876His