Canonical Allele Identifier: CA15425527
Gene: ZFAND3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.38139068T>C , CM000668.2:g.38139068T>C GRCh38
NC_000006.11:g.38106844T>C , CM000668.1:g.38106844T>C GRCh37
NC_000006.10:g.38214822T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000287218.9:c.530-13167T>C MANE Select ENSP00000287218.4:n.530-13167T>C
ENST00000287218.8:c.530-13167T>C ENSP00000287218.4:n.530-13167T>C
ENST00000373389.5:c.459-3191T>C
ENST00000373391.6:c.464-13167T>C ENSP00000362489.2:n.464-13167T>C
ENST00000440482.2:n.212-13167T>C
NM_021943.2:c.530-13167T>C NP_068762.1:n.530-13167T>C
XM_005249269.1:c.464-13167T>C XP_005249326.1:n.464-13167T>C
XM_006715155.2:c.530-12237T>C XP_006715218.1:n.530-12237T>C
XM_011514790.1:c.362-13167T>C XP_011513092.1:n.362-13167T>C
XR_926766.1:n.4495T>C
XM_005249269.2:c.464-13167T>C XP_005249326.1:n.464-13167T>C
XM_011514790.2:c.362-13167T>C XP_011513092.1:n.362-13167T>C
XM_017011171.2:c.482-13167T>C XP_016866660.1:n.482-13167T>C
NM_021943.3:c.530-13167T>C MANE Select NP_068762.1:n.530-13167T>C
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