Canonical Allele Identifier: CA352008718
Gene: CRTAP HGNC NCBI

Linked Data

gnomAD v4: 3-33114450-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.33114450G>A , CM000665.2:g.33114450G>A GRCh38
NC_000003.11:g.33155942G>A , CM000665.1:g.33155942G>A GRCh37
NC_000003.10:g.33130946G>A NCBI36
NG_008122.1:g.5493G>A , LRG_4:g.5493G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000320954.11:c.373G>A MANE Select ENSP00000323696.5:p.Gly125Ser
ENST00000320954.10:c.373G>A ENSP00000323696.5:p.Gly125Ser
ENST00000449224.1:c.373G>A ENSP00000409997.1:p.Gly125Ser
NM_006371.4:c.373G>A , LRG_4t1:c.373G>A NP_006362.1:p.Gly125Ser
NM_006371.5:c.373G>A MANE Select NP_006362.1:p.Gly125Ser
NM_001393363.1:c.373G>A NP_001380292.1:p.Gly125Ser
NM_001393364.1:c.373G>A NP_001380293.1:p.Gly125Ser
NM_001393365.1:c.373G>A NP_001380294.1:p.Gly125Ser