Canonical Allele Identifier: CA2300412

Gene: CRTAP

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33129938G>C , CM000665.2:g.33129938G>C	GRCh38
NC_000003.11:g.33171430G>C , CM000665.1:g.33171430G>C	GRCh37
NC_000003.10:g.33146434G>C	NCBI36
NG_008122.1:g.20981G>C , LRG_4:g.20981G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_006371.5:c.794-1G>C MANE Select	NP_006362.1:n.794-1G>C
ENST00000320954.11:c.794-1G>C MANE Select	ENSP00000323696.5:n.794-1G>C
NM_001393363.1:c.794-1G>C	NP_001380292.1:n.794-1G>C
NM_001393364.1:c.794-2617G>C	NP_001380293.1:n.794-2617G>C
NM_001393365.1:c.644-1G>C	NP_001380294.1:n.644-1G>C
NM_006371.4:c.794-1G>C , LRG_4t1:c.794-1G>C	NP_006362.1:n.794-1G>C
ENST00000320954.10:c.794-1G>C	ENSP00000323696.5:n.794-1G>C
ENST00000449224.1:c.794-2617G>C	ENSP00000409997.1:n.794-2617G>C
ENST00000485310.1:n.388-1G>C