Canonical Allele Identifier: CA375644089

Gene: NOTCH1

Linked Data

• MyVariant Identifiers: chr9:g.139399150C>G (hg19) ; chr9:g.136504698C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136504698C>G , CM000671.2:g.136504698C>G	GRCh38
NC_000009.11:g.139399150C>G , CM000671.1:g.139399150C>G	GRCh37
NC_000009.10:g.138518971C>G	NCBI36
NG_007458.1:g.46089G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645828.1:n.2800G>C
ENST00000651671.1:c.4993G>C MANE Select	ENSP00000498587.1:p.Glu1665Gln
ENST00000679595.1:c.4993G>C	ENSP00000506241.1:p.Glu1665Gln
ENST00000680133.1:c.4879G>C	ENSP00000505319.1:p.Glu1627Gln
ENST00000680218.1:c.4873G>C	ENSP00000505339.1:p.Glu1625Gln
ENST00000680668.1:c.4879G>C	ENSP00000506336.1:p.Glu1627Gln
ENST00000680778.1:c.2590G>C	ENSP00000506033.1:p.Glu864Gln
ENST00000680924.1:c.*2393G>C	ENSP00000506031.1:n.*2393G>C
ENST00000681135.1:c.*2602G>C	ENSP00000506636.1:n.*2602G>C
ENST00000681298.1:n.1806G>C
ENST00000681454.1:c.*4229G>C	ENSP00000505763.1:n.*4229G>C
ENST00000277541.6:c.4993G>C	ENSP00000277541.6:p.Glu1665Gln
ENST00000494783.1:n.148G>C
NM_017617.3:c.4993G>C	NP_060087.3:p.Glu1665Gln
XM_011518717.1:c.4294G>C	XP_011517019.1:p.Glu1432Gln
NM_017617.5:c.4993G>C MANE Select	NP_060087.3:p.Glu1665Gln
XM_011518717.2:c.4270G>C	XP_011517019.2:p.Glu1424Gln