Canonical Allele Identifier: CA436107368

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142168430A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142449588A>G , CM000665.2:g.142449588A>G	GRCh38
NC_000003.11:g.142168430A>G , CM000665.1:g.142168430A>G	GRCh37
NC_000003.10:g.143651120A>G	NCBI36
NG_008951.1:g.134239T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.7776T>C MANE Select	ENSP00000343741.4:p.Val2592=
ENST00000513291.2:n.6485T>C
ENST00000653893.1:n.2634T>C
ENST00000654170.1:n.2619T>C
ENST00000656114.1:n.2862T>C
ENST00000656590.1:c.6703T>C
ENST00000658083.1:n.2956T>C
ENST00000661310.1:c.7584T>C	ENSP00000499589.1:p.Val2528=
ENST00000665483.1:n.5316T>C
ENST00000666447.1:n.4279T>C
ENST00000666943.1:n.4508T>C
ENST00000350721.8:c.7776T>C	ENSP00000343741.4:p.Val2592=
ENST00000504521.5:c.365T>C	ENSP00000422553.1:n.365T>C
ENST00000513291.1:c.4840T>C
ENST00000515810.1:c.202T>C	ENSP00000421870.1:n.202T>C
NM_001184.3:c.7776T>C	NP_001175.2:p.Val2592=
XM_011512924.1:c.7782T>C	XP_011511226.1:p.Val2594=
XM_011512925.1:c.7590T>C	XP_011511227.1:p.Val2530=
XR_924147.1:n.10533T>C
XR_924148.1:n.8008T>C
NM_001354579.1:c.7584T>C	NP_001341508.1:p.Val2528=
XR_001740179.2:n.8002T>C
XR_924148.2:n.8008T>C
NM_001184.4:c.7776T>C MANE Select	NP_001175.2:p.Val2592=
NM_001354579.2:c.7584T>C	NP_001341508.1:p.Val2528=