Canonical Allele Identifier: CA354793726

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142168321C>A (hg19) ; chr3:g.142449479C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142449479C>A , CM000665.2:g.142449479C>A	GRCh38
NC_000003.11:g.142168321C>A , CM000665.1:g.142168321C>A	GRCh37
NC_000003.10:g.143651011C>A	NCBI36
NG_008951.1:g.134348G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.7885G>T MANE Select	ENSP00000343741.4:p.Asp2629Tyr
ENST00000513291.2:n.6594G>T
ENST00000653893.1:n.2743G>T
ENST00000654170.1:n.2728G>T
ENST00000656114.1:n.2971G>T
ENST00000656590.1:c.6812G>T
ENST00000658083.1:n.3065G>T
ENST00000661310.1:c.7693G>T	ENSP00000499589.1:p.Asp2565Tyr
ENST00000665483.1:n.5425G>T
ENST00000666447.1:n.4388G>T
ENST00000666943.1:n.4617G>T
ENST00000350721.8:c.7885G>T	ENSP00000343741.4:p.Asp2629Tyr
ENST00000504521.5:c.474G>T	ENSP00000422553.1:n.474G>T
ENST00000513291.1:c.4949G>T
ENST00000515810.1:c.311G>T	ENSP00000421870.1:n.311G>T
NM_001184.3:c.7885G>T	NP_001175.2:p.Asp2629Tyr
XM_011512924.1:c.7891G>T	XP_011511226.1:p.Asp2631Tyr
XM_011512925.1:c.7699G>T	XP_011511227.1:p.Asp2567Tyr
XR_924147.1:n.10642G>T
XR_924148.1:n.8117G>T
NM_001354579.1:c.7693G>T	NP_001341508.1:p.Asp2565Tyr
XR_001740179.2:n.8111G>T
XR_924148.2:n.8117G>T
NM_001184.4:c.7885G>T MANE Select	NP_001175.2:p.Asp2629Tyr
NM_001354579.2:c.7693G>T	NP_001341508.1:p.Asp2565Tyr