Canonical Allele Identifier: CA2667046067

Gene: ZDHHC23

Linked Data

• gnomAD v4: 3-113962041-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.113962041T>C , CM000665.2:g.113962041T>C	GRCh38
NC_000003.11:g.113680888T>C , CM000665.1:g.113680888T>C	GRCh37
NC_000003.10:g.115163578T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000638807.2:c.*3411T>C MANE Select	ENSP00000492287.2:n.*3411T>C
ENST00000638807.1:c.4122T>C	ENSP00000492287.1:n.4122T>C
ENST00000330212.7:c.*1308T>C	ENSP00000330485.3:n.*1308T>C
ENST00000478793.1:c.*1047T>C	ENSP00000420251.1:n.*1047T>C
ENST00000488129.1:n.3957T>C
ENST00000496083.1:c.86-3129T>C	ENSP00000417579.1:n.86-3129T>C
NM_173570.3:c.*1308T>C	NP_775841.2:n.*1308T>C
XM_005247265.1:c.*3411T>C	XP_005247322.1:n.*3411T>C
XM_005247266.1:c.*3411T>C	XP_005247323.1:n.*3411T>C
XM_005247269.1:c.*1308T>C	XP_005247326.1:n.*1308T>C
XM_005247270.2:c.*3411T>C	XP_005247327.1:n.*3411T>C
XM_006713561.1:c.*3411T>C	XP_006713624.1:n.*3411T>C
XM_006713562.2:c.1216+3503T>C	XP_006713625.1:n.1216+3503T>C
XM_011512618.1:c.*3411T>C	XP_011510920.1:n.*3411T>C
XM_011512619.1:c.*2498T>C	XP_011510921.1:n.*2498T>C
XM_011512620.1:c.*979T>C	XP_011510922.1:n.*979T>C
XR_241479.2:n.1459+3503T>C
XR_924118.1:n.1459+3503T>C
XR_924119.1:n.2861T>C
XR_924120.1:n.2529T>C
XR_924121.1:n.1539+2441T>C
NM_001320466.1:c.*3411T>C	NP_001307395.1:n.*3411T>C
NM_001320467.1:c.*3411T>C	NP_001307396.1:n.*3411T>C
NM_001320468.1:c.*3411T>C	NP_001307397.1:n.*3411T>C
NM_001363952.1:c.*2498T>C	NP_001350881.1:n.*2498T>C
NM_173570.4:c.*1308T>C	NP_775841.2:n.*1308T>C
NR_135271.1:n.2693T>C
XM_005247270.3:c.*3411T>C	XP_005247327.1:n.*3411T>C
XM_006713562.3:c.1216+3503T>C	XP_006713625.1:n.1216+3503T>C
XM_011512618.2:c.*3411T>C	XP_011510920.1:n.*3411T>C
XM_017006084.1:c.*3411T>C	XP_016861573.1:n.*3411T>C
XM_017006086.1:c.*1308T>C	XP_016861575.1:n.*1308T>C
XM_017006087.1:c.*2498T>C	XP_016861576.1:n.*2498T>C
XR_001740079.1:n.1459+3503T>C
XR_001740080.1:n.1439+3503T>C
XR_001740081.1:n.1539+2441T>C
XR_924118.3:n.1459+3503T>C
NM_001320466.2:c.*3411T>C MANE Select	NP_001307395.1:n.*3411T>C
NM_001320467.2:c.*3411T>C	NP_001307396.1:n.*3411T>C
NM_001320468.2:c.*3411T>C	NP_001307397.1:n.*3411T>C
NM_173570.5:c.*1308T>C	NP_775841.2:n.*1308T>C
NR_135271.2:n.2581T>C