Canonical Allele Identifier: CA401161044
Gene: AANAT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.76469324G>T , CM000679.2:g.76469324G>T GRCh38
NC_000017.10:g.74465406G>T , CM000679.1:g.74465406G>T GRCh37
NC_000017.9:g.71977001G>T NCBI36
NG_015976.1:g.20974G>T
NG_032852.1:g.37104C>A , LRG_532:g.37104C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000392492.8:c.315G>T MANE Select ENSP00000376282.2:p.Met105Ile
ENST00000250615.7:c.450G>T ENSP00000250615.2:p.Met150Ile
ENST00000392492.7:c.315G>T ENSP00000376282.2:p.Met105Ile
ENST00000585649.1:c.429G>T ENSP00000468717.1:p.Met143Ile
ENST00000587798.1:c.*92G>T ENSP00000468239.1:n.*92G>T
NM_001088.2:c.315G>T NP_001079.1:p.Met105Ile
NM_001166579.1:c.450G>T NP_001160051.1:p.Met150Ile
NR_110548.1:n.626G>T
XM_011524415.1:c.315G>T XP_011522717.1:p.Met105Ile
XM_011524416.1:c.522G>T XP_011522718.1:p.Met174Ile
XM_011524417.1:c.522G>T XP_011522719.1:p.Met174Ile
XM_011524418.1:c.522G>T XP_011522720.1:p.Met174Ile
XM_011524419.1:c.522G>T XP_011522721.1:p.Met174Ile
XM_011524420.1:c.522G>T XP_011522722.1:p.Met174Ile
XM_011524421.1:c.522G>T XP_011522723.1:p.Met174Ile
XM_011524422.1:c.405G>T XP_011522724.1:p.Met135Ile
XM_011524423.1:c.315G>T XP_011522725.1:p.Met105Ile
XM_017024259.1:c.429G>T XP_016879748.1:p.Met143Ile
NM_001088.3:c.315G>T MANE Select NP_001079.1:p.Met105Ile
NR_110548.2:n.571G>T
NM_001166579.2:c.450G>T NP_001160051.1:p.Met150Ile