Canonical Allele Identifier: CA436126402

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142272188A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142553346A>G , CM000665.2:g.142553346A>G	GRCh38
NC_000003.11:g.142272188A>G , CM000665.1:g.142272188A>G	GRCh37
NC_000003.10:g.143754878A>G	NCBI36
NG_008951.1:g.30481T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.2686T>C MANE Select	ENSP00000343741.4:p.Leu896=
ENST00000515149.3:c.*1460T>C	ENSP00000425897.3:n.*1460T>C
ENST00000653868.1:n.2715T>C
ENST00000656590.1:c.1476T>C
ENST00000659195.1:n.5561T>C
ENST00000661310.1:c.2494T>C	ENSP00000499589.1:p.Leu832=
ENST00000350721.8:c.2686T>C	ENSP00000343741.4:p.Leu896=
NM_001184.3:c.2686T>C	NP_001175.2:p.Leu896=
XM_011512924.1:c.2686T>C	XP_011511226.1:p.Leu896=
XM_011512925.1:c.2494T>C	XP_011511227.1:p.Leu832=
XM_011512926.1:c.2686T>C	XP_011511228.1:p.Leu896=
XM_011512927.1:c.2686T>C	XP_011511229.1:p.Leu896=
XR_924147.1:n.2775T>C
XR_924148.1:n.2775T>C
XR_924149.1:n.2775T>C
NM_001354579.1:c.2494T>C	NP_001341508.1:p.Leu832=
XR_001740179.2:n.2775T>C
XR_001740180.2:n.2775T>C
XR_001740181.2:n.2775T>C
XR_001740182.1:n.2775T>C
XR_002959543.1:n.2775T>C
XR_924148.2:n.2775T>C
NM_001184.4:c.2686T>C MANE Select	NP_001175.2:p.Leu896=
NM_001354579.2:c.2494T>C	NP_001341508.1:p.Leu832=