Canonical Allele Identifier: CA4326573

Gene: CROT

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87392772A>G , CM000669.2:g.87392772A>G	GRCh38
NC_000007.13:g.87022088A>G , CM000669.1:g.87022088A>G	GRCh37
NC_000007.12:g.86860024A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331536.8:c.1547A>G MANE Select	ENSP00000331981.4:p.Glu516Gly
ENST00000331536.7:c.1547A>G	ENSP00000331981.3:p.Glu516Gly
ENST00000419147.6:c.1631A>G	ENSP00000413575.2:p.Glu544Gly
ENST00000442291.1:c.1547A>G	ENSP00000411983.1:p.Glu516Gly
NM_001143935.1:c.1631A>G	NP_001137407.1:p.Glu544Gly
NM_021151.3:c.1547A>G	NP_066974.2:p.Glu516Gly
XM_011516337.1:c.1547A>G	XP_011514639.1:p.Glu516Gly
XM_011516337.3:c.1547A>G	XP_011514639.1:p.Glu516Gly
XM_017012370.1:c.716A>G	XP_016867859.1:p.Glu239Gly
NM_001143935.2:c.1631A>G	NP_001137407.1:p.Glu544Gly
NM_021151.4:c.1547A>G MANE Select	NP_066974.2:p.Glu516Gly