Canonical Allele Identifier: CA401065198

Gene: ACOX1

Linked Data

• MyVariant Identifiers: chr17:g.73949554G>A (hg19) ; chr17:g.75953473G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75953473G>A , CM000679.2:g.75953473G>A	GRCh38
NC_000017.10:g.73949554G>A , CM000679.1:g.73949554G>A	GRCh37
NC_000017.9:g.71461149G>A	NCBI36
NG_008190.1:g.30891C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301608.9:c.922C>T	ENSP00000301608.4:p.His308Tyr
ENST00000293217.10:c.922C>T MANE Select	ENSP00000293217.4:p.His308Tyr
ENST00000293217.9:c.922C>T	ENSP00000293217.4:p.His308Tyr
ENST00000301608.8:c.922C>T	ENSP00000301608.4:p.His308Tyr
ENST00000572047.5:c.1096C>T	ENSP00000459936.1:n.1096C>T
ENST00000573078.5:c.*411C>T	ENSP00000458325.1:n.*411C>T
ENST00000589744.1:n.172C>T
NM_001185039.1:c.808C>T	NP_001171968.1:p.His270Tyr
NM_004035.6:c.922C>T	NP_004026.2:p.His308Tyr
NM_007292.5:c.922C>T	NP_009223.2:p.His308Tyr
XM_011524868.1:c.718C>T	XP_011523170.1:p.His240Tyr
XM_011524869.1:c.514C>T	XP_011523171.1:p.His172Tyr
XM_011524868.3:c.718C>T	XP_011523170.1:p.His240Tyr
XM_011524869.3:c.514C>T	XP_011523171.1:p.His172Tyr
NM_004035.7:c.922C>T MANE Select	NP_004026.2:p.His308Tyr
NM_001185039.2:c.808C>T	NP_001171968.1:p.His270Tyr
NM_007292.6:c.922C>T	NP_009223.2:p.His308Tyr