Canonical Allele Identifier: CA354805491

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142188929T>G (hg19) ; chr3:g.142470087T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470087T>G , CM000665.2:g.142470087T>G	GRCh38
NC_000003.11:g.142188929T>G , CM000665.1:g.142188929T>G	GRCh37
NC_000003.10:g.143671619T>G	NCBI36
NG_008951.1:g.113740A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.6318A>C MANE Select	ENSP00000343741.4:p.Lys2106Asn
ENST00000513291.2:n.1502A>C
ENST00000654170.1:n.1161A>C
ENST00000656590.1:c.5108A>C
ENST00000661310.1:c.6126A>C	ENSP00000499589.1:p.Lys2042Asn
ENST00000665483.1:n.173A>C
ENST00000666447.1:n.153A>C
ENST00000666943.1:n.1782A>C
ENST00000350721.8:c.6318A>C	ENSP00000343741.4:p.Lys2106Asn
NM_001184.3:c.6318A>C	NP_001175.2:p.Lys2106Asn
XM_011512924.1:c.6324A>C	XP_011511226.1:p.Lys2108Asn
XM_011512925.1:c.6132A>C	XP_011511227.1:p.Lys2044Asn
XR_924147.1:n.6413A>C
XR_924148.1:n.6413A>C
XR_924149.1:n.6292A>C
NM_001354579.1:c.6126A>C	NP_001341508.1:p.Lys2042Asn
XR_001740179.2:n.6407A>C
XR_001740180.2:n.6461A>C
XR_001740181.2:n.6340A>C
XR_001740182.1:n.6292A>C
XR_002959543.1:n.6517A>C
XR_924148.2:n.6413A>C
NM_001184.4:c.6318A>C MANE Select	NP_001175.2:p.Lys2106Asn
NM_001354579.2:c.6126A>C	NP_001341508.1:p.Lys2042Asn