Canonical Allele Identifier: CA1742780766

Gene: AHCYL2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.129365012G= , CM000669.2:g.129365012G=	GRCh38
NC_000007.13:g.129004853G= , CM000669.1:g.129004853G=	GRCh37
NC_000007.12:g.128792089G=	NCBI36
NG_029180.1:g.144999G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000325006.8:c.364-14626G= MANE Select	ENSP00000315931.3:n.364-14626G=
ENST00000325006.7:c.364-14626G=	ENSP00000315931.3:n.364-14626G=
ENST00000446544.6:c.364-14629G=	ENSP00000413639.2:n.364-14629G=
ENST00000461161.5:n.159+13351G=
NM_001130720.2:c.364-14629G=	NP_001124192.1:n.364-14629G=
NM_015328.3:c.364-14626G=	NP_056143.1:n.364-14626G=
XR_927961.1:n.86-1539C=
XM_017011904.1:c.-255-14629G=	XP_016867393.1:n.-255-14629G=
XM_017011906.1:c.-258-14626G=	XP_016867395.1:n.-258-14626G=
NM_001130720.3:c.364-14629G=	NP_001124192.1:n.364-14629G=
NM_015328.4:c.364-14626G= MANE Select	NP_056143.1:n.364-14626G=
NM_001393387.1:c.364-14626G=	NP_001380316.1:n.364-14626G=
NR_171671.1:n.411-12530G=