Canonical Allele Identifier: CA354823537

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142281084A>G (hg19) ; chr3:g.142562242A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142562242A>G , CM000665.2:g.142562242A>G	GRCh38
NC_000003.11:g.142281084A>G , CM000665.1:g.142281084A>G	GRCh37
NC_000003.10:g.143763774A>G	NCBI36
NG_008951.1:g.21585T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.1160T>C MANE Select	ENSP00000343741.4:p.Val387Ala
ENST00000515149.3:c.293-821T>C	ENSP00000425897.3:n.293-821T>C
ENST00000653868.1:n.1189T>C
ENST00000657914.1:n.3518T>C
ENST00000659195.1:n.3225T>C
ENST00000661310.1:c.1160T>C	ENSP00000499589.1:p.Val387Ala
ENST00000350721.8:c.1160T>C	ENSP00000343741.4:p.Val387Ala
ENST00000507148.1:c.*96T>C	ENSP00000426595.1:n.*96T>C
ENST00000515149.2:c.203T>C	ENSP00000425897.2:p.Val68Ala
NM_001184.3:c.1160T>C	NP_001175.2:p.Val387Ala
XM_011512924.1:c.1160T>C	XP_011511226.1:p.Val387Ala
XM_011512925.1:c.1160T>C	XP_011511227.1:p.Val387Ala
XM_011512926.1:c.1160T>C	XP_011511228.1:p.Val387Ala
XM_011512927.1:c.1160T>C	XP_011511229.1:p.Val387Ala
XR_924147.1:n.1249T>C
XR_924148.1:n.1249T>C
XR_924149.1:n.1249T>C
NM_001354579.1:c.1160T>C	NP_001341508.1:p.Val387Ala
XR_001740179.2:n.1249T>C
XR_001740180.2:n.1249T>C
XR_001740181.2:n.1249T>C
XR_001740182.1:n.1249T>C
XR_002959543.1:n.1249T>C
XR_924148.2:n.1249T>C
NM_001184.4:c.1160T>C MANE Select	NP_001175.2:p.Val387Ala
NM_001354579.2:c.1160T>C	NP_001341508.1:p.Val387Ala