Canonical Allele Identifier: CA375631621

Gene: NOTCH1

Linked Data

• MyVariant Identifiers: chr9:g.139391725T>G (hg19) ; chr9:g.136497273T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136497273T>G , CM000671.2:g.136497273T>G	GRCh38
NC_000009.11:g.139391725T>G , CM000671.1:g.139391725T>G	GRCh37
NC_000009.10:g.138511546T>G	NCBI36
NG_007458.1:g.53514A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651671.1:c.6466A>C MANE Select	ENSP00000498587.1:p.Lys2156Gln
ENST00000679595.1:c.*1506A>C	ENSP00000506241.1:n.*1506A>C
ENST00000679969.1:n.3062A>C
ENST00000680003.1:n.2798A>C
ENST00000680133.1:c.6352A>C	ENSP00000505319.1:p.Lys2118Gln
ENST00000680218.1:c.6346A>C	ENSP00000505339.1:p.Lys2116Gln
ENST00000680668.1:c.6352A>C	ENSP00000506336.1:p.Lys2118Gln
ENST00000680778.1:c.4063A>C	ENSP00000506033.1:p.Lys1355Gln
ENST00000680924.1:c.*3866A>C	ENSP00000506031.1:n.*3866A>C
ENST00000681135.1:c.*4075A>C	ENSP00000506636.1:n.*4075A>C
ENST00000681298.1:n.4571A>C
ENST00000681454.1:c.*5702A>C	ENSP00000505763.1:n.*5702A>C
ENST00000277541.6:c.6466A>C	ENSP00000277541.6:p.Lys2156Gln
NM_017617.3:c.6466A>C	NP_060087.3:p.Lys2156Gln
XM_011518717.1:c.5767A>C	XP_011517019.1:p.Lys1923Gln
NM_017617.5:c.6466A>C MANE Select	NP_060087.3:p.Lys2156Gln
XM_011518717.2:c.5743A>C	XP_011517019.2:p.Lys1915Gln