Canonical Allele Identifier: CA467832570

Gene: NOTCH1

Linked Data

• MyVariant Identifiers: chr9:g.139391777C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136497325C>G , CM000671.2:g.136497325C>G	GRCh38
NC_000009.11:g.139391777C>G , CM000671.1:g.139391777C>G	GRCh37
NC_000009.10:g.138511598C>G	NCBI36
NG_007458.1:g.53462G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651671.1:c.6414G>C MANE Select	ENSP00000498587.1:p.Pro2138=
ENST00000679595.1:c.*1454G>C	ENSP00000506241.1:n.*1454G>C
ENST00000679969.1:n.3010G>C
ENST00000680003.1:n.2746G>C
ENST00000680133.1:c.6300G>C	ENSP00000505319.1:p.Pro2100=
ENST00000680218.1:c.6294G>C	ENSP00000505339.1:p.Pro2098=
ENST00000680668.1:c.6300G>C	ENSP00000506336.1:p.Pro2100=
ENST00000680778.1:c.4011G>C	ENSP00000506033.1:p.Pro1337=
ENST00000680924.1:c.*3814G>C	ENSP00000506031.1:n.*3814G>C
ENST00000681135.1:c.*4023G>C	ENSP00000506636.1:n.*4023G>C
ENST00000681298.1:n.4519G>C
ENST00000681454.1:c.*5650G>C	ENSP00000505763.1:n.*5650G>C
ENST00000277541.6:c.6414G>C	ENSP00000277541.6:p.Pro2138=
NM_017617.3:c.6414G>C	NP_060087.3:p.Pro2138=
XM_011518717.1:c.5715G>C	XP_011517019.1:p.Pro1905=
NM_017617.5:c.6414G>C MANE Select	NP_060087.3:p.Pro2138=
XM_011518717.2:c.5691G>C	XP_011517019.2:p.Pro1897=