Canonical Allele Identifier: CA1742780699

Gene: AHCYL2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.129364833_129364834delinsAT , CM000669.2:g.129364833_129364834delinsAT	GRCh38
NC_000007.13:g.129004674_129004675delinsAT , CM000669.1:g.129004674_129004675delinsAT	GRCh37
NC_000007.12:g.128791910_128791911delinsAT	NCBI36
NG_029180.1:g.144820_144821delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325006.8:c.364-14805_364-14804delinsAT MANE Select	ENSP00000315931.3:n.364-14805_364-14804delinsAT
ENST00000325006.7:c.364-14805_364-14804delinsAT	ENSP00000315931.3:n.364-14805_364-14804delinsAT
ENST00000446544.6:c.364-14808_364-14807delinsAT	ENSP00000413639.2:n.364-14808_364-14807delinsAT
ENST00000461161.5:n.159+13172_159+13173delinsAT
NM_001130720.2:c.364-14808_364-14807delinsAT	NP_001124192.1:n.364-14808_364-14807delinsAT
NM_015328.3:c.364-14805_364-14804delinsAT	NP_056143.1:n.364-14805_364-14804delinsAT
XR_927961.1:n.86-1361_86-1360delinsAT
XM_017011904.1:c.-255-14808_-255-14807delinsAT	XP_016867393.1:n.-255-14808_-255-14807delinsAT
XM_017011906.1:c.-258-14805_-258-14804delinsAT	XP_016867395.1:n.-258-14805_-258-14804delinsAT
NM_001130720.3:c.364-14808_364-14807delinsAT	NP_001124192.1:n.364-14808_364-14807delinsAT
NM_015328.4:c.364-14805_364-14804delinsAT MANE Select	NP_056143.1:n.364-14805_364-14804delinsAT
NM_001393387.1:c.364-14805_364-14804delinsAT	NP_001380316.1:n.364-14805_364-14804delinsAT
NR_171671.1:n.411-12709_411-12708delinsAT