Canonical Allele Identifier: CA368053956

Gene: CROT

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87392985G>T , CM000669.2:g.87392985G>T	GRCh38
NC_000007.13:g.87022301G>T , CM000669.1:g.87022301G>T	GRCh37
NC_000007.12:g.86860237G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331536.8:c.1636G>T MANE Select	ENSP00000331981.4:p.Val546Phe
ENST00000331536.7:c.1636G>T	ENSP00000331981.3:p.Val546Phe
ENST00000419147.6:c.1720G>T	ENSP00000413575.2:p.Val574Phe
ENST00000442291.1:c.1636G>T	ENSP00000411983.1:p.Val546Phe
NM_001143935.1:c.1720G>T	NP_001137407.1:p.Val574Phe
NM_021151.3:c.1636G>T	NP_066974.2:p.Val546Phe
XM_011516337.1:c.1636G>T	XP_011514639.1:p.Val546Phe
XM_011516337.3:c.1636G>T	XP_011514639.1:p.Val546Phe
XM_017012370.1:c.805G>T	XP_016867859.1:p.Val269Phe
NM_001143935.2:c.1720G>T	NP_001137407.1:p.Val574Phe
NM_021151.4:c.1636G>T MANE Select	NP_066974.2:p.Val546Phe