Canonical Allele Identifier: CA354804144

Gene: ATR

Linked Data

• dbSNP Id: rs2108278563
• MyVariant Identifiers: chr3:g.142188193T>G (hg19) ; chr3:g.142469351T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142469351T>G , CM000665.2:g.142469351T>G	GRCh38
NC_000003.11:g.142188193T>G , CM000665.1:g.142188193T>G	GRCh37
NC_000003.10:g.143670883T>G	NCBI36
NG_008951.1:g.114476A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6538A>C MANE Select	ENSP00000343741.4:p.Thr2180Pro
ENST00000513291.2:n.1722A>C
ENST00000654170.1:n.1381A>C
ENST00000656590.1:c.5328A>C
ENST00000661310.1:c.6346A>C	ENSP00000499589.1:p.Thr2116Pro
ENST00000665483.1:n.393A>C
ENST00000666447.1:n.373A>C
ENST00000666943.1:n.2002A>C
ENST00000350721.8:c.6538A>C	ENSP00000343741.4:p.Thr2180Pro
ENST00000513291.1:c.77A>C
NM_001184.3:c.6538A>C	NP_001175.2:p.Thr2180Pro
XM_011512924.1:c.6544A>C	XP_011511226.1:p.Thr2182Pro
XM_011512925.1:c.6352A>C	XP_011511227.1:p.Thr2118Pro
XR_924147.1:n.6633A>C
XR_924148.1:n.6633A>C
XR_924149.1:n.6512A>C
NM_001354579.1:c.6346A>C	NP_001341508.1:p.Thr2116Pro
XR_001740179.2:n.6627A>C
XR_924148.2:n.6633A>C
NM_001184.4:c.6538A>C MANE Select	NP_001175.2:p.Thr2180Pro
NM_001354579.2:c.6346A>C	NP_001341508.1:p.Thr2116Pro