Canonical Allele Identifier: CA833193190

Gene: AHCYL2

Linked Data

• dbSNP Id: rs1336180865
• MyVariant Identifiers: chr7:g.129004796_129004797del (hg19) ; chr7:g.129364955_129364956del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.129364957_129364958del , CM000669.2:g.129364957_129364958del	GRCh38
NC_000007.13:g.129004798_129004799del , CM000669.1:g.129004798_129004799del	GRCh37
NC_000007.12:g.128792034_128792035del	NCBI36
NG_029180.1:g.144944_144945del

Transcript Alleles

HGVS	Amino-acid change
ENST00000325006.8:c.364-14681_364-14680del MANE Select	ENSP00000315931.3:n.364-14681_364-14680de...
ENST00000325006.7:c.364-14681_364-14680del	ENSP00000315931.3:n.364-14681_364-14680de...
ENST00000446544.6:c.364-14684_364-14683del	ENSP00000413639.2:n.364-14684_364-14683de...
ENST00000461161.5:n.159+13296_159+13297del
NM_001130720.2:c.364-14684_364-14683del	NP_001124192.1:n.364-14684_364-14683del
NM_015328.3:c.364-14681_364-14680del	NP_056143.1:n.364-14681_364-14680del
XR_927961.1:n.86-1483_86-1482del
XM_017011904.1:c.-255-14684_-255-14683del	XP_016867393.1:n.-255-14684_-255-14683del...
XM_017011906.1:c.-258-14681_-258-14680del	XP_016867395.1:n.-258-14681_-258-14680del...
NM_001130720.3:c.364-14684_364-14683del	NP_001124192.1:n.364-14684_364-14683del
NM_015328.4:c.364-14681_364-14680del MANE Select	NP_056143.1:n.364-14681_364-14680del
NM_001393387.1:c.364-14681_364-14680del	NP_001380316.1:n.364-14681_364-14680del
NR_171671.1:n.411-12585_411-12584del