Canonical Allele Identifier: CA1742780729
Gene: AHCYL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.129364896_129364901delinsTATAAC , CM000669.2:g.129364896_129364901delinsTATAAC GRCh38
NC_000007.13:g.129004737_129004742delinsTATAAC , CM000669.1:g.129004737_129004742delinsTATAAC GRCh37
NC_000007.12:g.128791973_128791978delinsTATAAC NCBI36
NG_029180.1:g.144883_144888delinsTATAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000325006.8:c.364-14742_364-14737delinsTATAAC MANE Select ENSP00000315931.3:n.364-14742_364-14737delinsTATAAC
ENST00000325006.7:c.364-14742_364-14737delinsTATAAC ENSP00000315931.3:n.364-14742_364-14737delinsTATAAC
ENST00000446544.6:c.364-14745_364-14740delinsTATAAC ENSP00000413639.2:n.364-14745_364-14740delinsTATAAC
ENST00000461161.5:n.159+13235_159+13240delinsTATAAC
NM_001130720.2:c.364-14745_364-14740delinsTATAAC NP_001124192.1:n.364-14745_364-14740delinsTATAAC
NM_015328.3:c.364-14742_364-14737delinsTATAAC NP_056143.1:n.364-14742_364-14737delinsTATAAC
XR_927961.1:n.86-1428_86-1423delinsGTTATA
XM_017011904.1:c.-255-14745_-255-14740delinsTATAAC XP_016867393.1:n.-255-14745_-255-14740delinsTATAAC
XM_017011906.1:c.-258-14742_-258-14737delinsTATAAC XP_016867395.1:n.-258-14742_-258-14737delinsTATAAC
NM_001130720.3:c.364-14745_364-14740delinsTATAAC NP_001124192.1:n.364-14745_364-14740delinsTATAAC
NM_015328.4:c.364-14742_364-14737delinsTATAAC MANE Select NP_056143.1:n.364-14742_364-14737delinsTATAAC
NM_001393387.1:c.364-14742_364-14737delinsTATAAC NP_001380316.1:n.364-14742_364-14737delinsTATAAC
NR_171671.1:n.411-12646_411-12641delinsTATAAC