Canonical Allele Identifier: CA1742780789
Gene: AHCYL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.129365054T= , CM000669.2:g.129365054T= GRCh38
NC_000007.13:g.129004895T= , CM000669.1:g.129004895T= GRCh37
NC_000007.12:g.128792131T= NCBI36
NG_029180.1:g.145041T=

Transcript Alleles

HGVS Amino-acid change
ENST00000325006.8:c.364-14584T= MANE Select ENSP00000315931.3:n.364-14584T=
ENST00000325006.7:c.364-14584T= ENSP00000315931.3:n.364-14584T=
ENST00000446544.6:c.364-14587T= ENSP00000413639.2:n.364-14587T=
ENST00000461161.5:n.159+13393T=
NM_001130720.2:c.364-14587T= NP_001124192.1:n.364-14587T=
NM_015328.3:c.364-14584T= NP_056143.1:n.364-14584T=
XR_927961.1:n.86-1581A=
XM_017011904.1:c.-255-14587T= XP_016867393.1:n.-255-14587T=
XM_017011906.1:c.-258-14584T= XP_016867395.1:n.-258-14584T=
NM_001130720.3:c.364-14587T= NP_001124192.1:n.364-14587T=
NM_015328.4:c.364-14584T= MANE Select NP_056143.1:n.364-14584T=
NM_001393387.1:c.364-14584T= NP_001380316.1:n.364-14584T=
NR_171671.1:n.411-12488T=