Canonical Allele Identifier: CA354805577

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142188948T>G (hg19) ; chr3:g.142470106T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470106T>G , CM000665.2:g.142470106T>G	GRCh38
NC_000003.11:g.142188948T>G , CM000665.1:g.142188948T>G	GRCh37
NC_000003.10:g.143671638T>G	NCBI36
NG_008951.1:g.113721A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6299A>C MANE Select	ENSP00000343741.4:p.Lys2100Thr
ENST00000513291.2:n.1483A>C
ENST00000654170.1:n.1142A>C
ENST00000656590.1:c.5089A>C
ENST00000661310.1:c.6107A>C	ENSP00000499589.1:p.Lys2036Thr
ENST00000665483.1:n.154A>C
ENST00000666447.1:n.134A>C
ENST00000666943.1:n.1763A>C
ENST00000350721.8:c.6299A>C	ENSP00000343741.4:p.Lys2100Thr
NM_001184.3:c.6299A>C	NP_001175.2:p.Lys2100Thr
XM_011512924.1:c.6305A>C	XP_011511226.1:p.Lys2102Thr
XM_011512925.1:c.6113A>C	XP_011511227.1:p.Lys2038Thr
XR_924147.1:n.6394A>C
XR_924148.1:n.6394A>C
XR_924149.1:n.6273A>C
NM_001354579.1:c.6107A>C	NP_001341508.1:p.Lys2036Thr
XR_001740179.2:n.6388A>C
XR_001740180.2:n.6442A>C
XR_001740181.2:n.6321A>C
XR_001740182.1:n.6273A>C
XR_002959543.1:n.6498A>C
XR_924148.2:n.6394A>C
NM_001184.4:c.6299A>C MANE Select	NP_001175.2:p.Lys2100Thr
NM_001354579.2:c.6107A>C	NP_001341508.1:p.Lys2036Thr