Canonical Allele Identifier: CA1742780749

Gene: AHCYL2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.129364936C= , CM000669.2:g.129364936C=	GRCh38
NC_000007.13:g.129004777C= , CM000669.1:g.129004777C=	GRCh37
NC_000007.12:g.128792013C=	NCBI36
NG_029180.1:g.144923C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000325006.8:c.364-14702C= MANE Select	ENSP00000315931.3:n.364-14702C=
ENST00000325006.7:c.364-14702C=	ENSP00000315931.3:n.364-14702C=
ENST00000446544.6:c.364-14705C=	ENSP00000413639.2:n.364-14705C=
ENST00000461161.5:n.159+13275C=
NM_001130720.2:c.364-14705C=	NP_001124192.1:n.364-14705C=
NM_015328.3:c.364-14702C=	NP_056143.1:n.364-14702C=
XR_927961.1:n.86-1463G=
XM_017011904.1:c.-255-14705C=	XP_016867393.1:n.-255-14705C=
XM_017011906.1:c.-258-14702C=	XP_016867395.1:n.-258-14702C=
NM_001130720.3:c.364-14705C=	NP_001124192.1:n.364-14705C=
NM_015328.4:c.364-14702C= MANE Select	NP_056143.1:n.364-14702C=
NM_001393387.1:c.364-14702C=	NP_001380316.1:n.364-14702C=
NR_171671.1:n.411-12606C=