Canonical Allele Identifier: CA660279993

Gene: ATRNL1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.115753077T>A , CM000672.2:g.115753077T>A	GRCh38
NC_000010.10:g.117512588T>A , CM000672.1:g.117512588T>A	GRCh37
NC_000010.9:g.117502578T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355044.8:c.3903+25722T>A MANE Select	ENSP00000347152.3:n.3903+25722T>A
ENST00000650603.1:c.3795+25722T>A	ENSP00000497485.1:n.3795+25722T>A
ENST00000355044.7:c.3903+25722T>A	ENSP00000347152.3:n.3903+25722T>A
NM_207303.4:c.3903+25722T>A MANE Select	NP_997186.1:n.3903+25722T>A
XM_011539586.1:c.3903+25722T>A	XP_011537888.1:n.3903+25722T>A
XM_011539587.1:c.3765+25722T>A	XP_011537889.1:n.3765+25722T>A
XM_011539588.1:c.3702+25722T>A	XP_011537890.1:n.3702+25722T>A
XM_011539590.1:c.3465+25722T>A	XP_011537892.1:n.3465+25722T>A
XM_011539591.1:c.3465+25722T>A	XP_011537893.1:n.3465+25722T>A
XR_945653.1:n.4284+25722T>A
XM_011539588.2:c.3702+25722T>A	XP_011537890.1:n.3702+25722T>A
XM_011539590.2:c.3465+25722T>A	XP_011537892.1:n.3465+25722T>A
XM_011539591.2:c.3465+25722T>A	XP_011537893.1:n.3465+25722T>A
XM_017016035.2:c.3903+25722T>A	XP_016871524.1:n.3903+25722T>A
XM_017016037.1:c.2622+25722T>A	XP_016871526.1:n.2622+25722T>A
XM_017016038.1:c.2484+25722T>A	XP_016871527.1:n.2484+25722T>A
XM_017016039.2:c.2307+25722T>A	XP_016871528.1:n.2307+25722T>A
XM_017016040.1:c.1968+25722T>A	XP_016871529.1:n.1968+25722T>A
XR_001747080.1:n.4231+25722T>A
XR_945653.2:n.4284+25722T>A