Canonical Allele Identifier: CA375634350

Gene: NOTCH1

Linked Data

• MyVariant Identifiers: chr9:g.139393597A>C (hg19) ; chr9:g.136499145A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136499145A>C , CM000671.2:g.136499145A>C	GRCh38
NC_000009.11:g.139393597A>C , CM000671.1:g.139393597A>C	GRCh37
NC_000009.10:g.138513418A>C	NCBI36
NG_007458.1:g.51642T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651671.1:c.6049T>G MANE Select	ENSP00000498587.1:p.Ser2017Ala
ENST00000679595.1:c.*1089T>G	ENSP00000506241.1:n.*1089T>G
ENST00000679969.1:n.2530T>G
ENST00000680003.1:n.2381T>G
ENST00000680133.1:c.5935T>G	ENSP00000505319.1:p.Ser1979Ala
ENST00000680218.1:c.5929T>G	ENSP00000505339.1:p.Ser1977Ala
ENST00000680668.1:c.5935T>G	ENSP00000506336.1:p.Ser1979Ala
ENST00000680778.1:c.3646T>G	ENSP00000506033.1:p.Ser1216Ala
ENST00000680924.1:c.*3449T>G	ENSP00000506031.1:n.*3449T>G
ENST00000681135.1:c.*3658T>G	ENSP00000506636.1:n.*3658T>G
ENST00000681298.1:n.4154T>G
ENST00000681454.1:c.*5285T>G	ENSP00000505763.1:n.*5285T>G
ENST00000277541.6:c.6049T>G	ENSP00000277541.6:p.Ser2017Ala
NM_017617.3:c.6049T>G	NP_060087.3:p.Ser2017Ala
XM_011518717.1:c.5350T>G	XP_011517019.1:p.Ser1784Ala
NM_017617.5:c.6049T>G MANE Select	NP_060087.3:p.Ser2017Ala
XM_011518717.2:c.5326T>G	XP_011517019.2:p.Ser1776Ala