Canonical Allele Identifier: CA2581601820
Gene: ZBTB24 HGNC NCBI
MICAL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.109462738A>T , CM000668.2:g.109462738A>T GRCh38
NC_000006.11:g.109783941A>T , CM000668.1:g.109783941A>T GRCh37
NC_000006.10:g.109890634A>T NCBI36
NG_029388.1:g.25500T>A , LRG_326:g.25500T>A
NG_042833.1:g.8231T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000698513.1:c.*3113T>A (ZBTB24) ENSP00000513763.1:n.*3113T>A
ENST00000698514.1:c.*4065T>A (ZBTB24) ENSP00000513764.1:n.*4065T>A
ENST00000698515.1:c.*4065T>A (ZBTB24) ENSP00000513765.1:n.*4065T>A
ENST00000698516.1:c.*3113T>A (ZBTB24) ENSP00000513766.1:n.*3113T>A
ENST00000230122.4:c.*3113T>A (ZBTB24) MANE Select ENSP00000230122.4:n.*3113T>A
ENST00000230122.3:c.*3113T>A (ZBTB24) ENSP00000230122.3:n.*3113T>A
ENST00000630715.2:c.14+2926T>A (MICAL1) ENSP00000486901.1:n.14+2926T>A
NM_001286613.1:c.14+2926T>A (MICAL1) NP_001273542.1:n.14+2926T>A
NM_014797.2:c.*3113T>A , LRG_326t1:c.*3113T>A (ZBTB24) NP_055612.2:n.*3113T>A
NM_014797.3:c.*3113T>A (ZBTB24) MANE Select NP_055612.2:n.*3113T>A
NM_001286613.2:c.14+2926T>A (MICAL1) NP_001273542.1:n.14+2926T>A