Canonical Allele Identifier: CA368041997

Gene: CROT

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87377392G>A , CM000669.2:g.87377392G>A	GRCh38
NC_000007.13:g.87006708G>A , CM000669.1:g.87006708G>A	GRCh37
NC_000007.12:g.86844644G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331536.8:c.920G>A MANE Select	ENSP00000331981.4:p.Gly307Asp
ENST00000331536.7:c.920G>A	ENSP00000331981.3:p.Gly307Asp
ENST00000419147.6:c.1004G>A	ENSP00000413575.2:p.Gly335Asp
ENST00000442291.1:c.920G>A	ENSP00000411983.1:p.Gly307Asp
ENST00000479014.1:n.125G>A
NM_001143935.1:c.1004G>A	NP_001137407.1:p.Gly335Asp
NM_021151.3:c.920G>A	NP_066974.2:p.Gly307Asp
XM_011516337.1:c.920G>A	XP_011514639.1:p.Gly307Asp
XM_011516337.3:c.920G>A	XP_011514639.1:p.Gly307Asp
XM_017012370.1:c.89G>A	XP_016867859.1:p.Gly30Asp
NM_001143935.2:c.1004G>A	NP_001137407.1:p.Gly335Asp
NM_021151.4:c.920G>A MANE Select	NP_066974.2:p.Gly307Asp