Canonical Allele Identifier: CA375634147

Gene: NOTCH1

Linked Data

• MyVariant Identifiers: chr9:g.139393446T>A (hg19) ; chr9:g.136498994T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136498994T>A , CM000671.2:g.136498994T>A	GRCh38
NC_000009.11:g.139393446T>A , CM000671.1:g.139393446T>A	GRCh37
NC_000009.10:g.138513267T>A	NCBI36
NG_007458.1:g.51793A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651671.1:c.6085A>T MANE Select	ENSP00000498587.1:p.Lys2029Ter
ENST00000679595.1:c.*1125A>T	ENSP00000506241.1:n.*1125A>T
ENST00000679969.1:n.2681A>T
ENST00000680003.1:n.2417A>T
ENST00000680133.1:c.5971A>T	ENSP00000505319.1:p.Lys1991Ter
ENST00000680218.1:c.5965A>T	ENSP00000505339.1:p.Lys1989Ter
ENST00000680668.1:c.5971A>T	ENSP00000506336.1:p.Lys1991Ter
ENST00000680778.1:c.3682A>T	ENSP00000506033.1:p.Lys1228Ter
ENST00000680924.1:c.*3485A>T	ENSP00000506031.1:n.*3485A>T
ENST00000681135.1:c.*3694A>T	ENSP00000506636.1:n.*3694A>T
ENST00000681298.1:n.4190A>T
ENST00000681454.1:c.*5321A>T	ENSP00000505763.1:n.*5321A>T
ENST00000277541.6:c.6085A>T	ENSP00000277541.6:p.Lys2029Ter
NM_017617.3:c.6085A>T	NP_060087.3:p.Lys2029Ter
XM_011518717.1:c.5386A>T	XP_011517019.1:p.Lys1796Ter
NM_017617.5:c.6085A>T MANE Select	NP_060087.3:p.Lys2029Ter
XM_011518717.2:c.5362A>T	XP_011517019.2:p.Lys1788Ter