Canonical Allele Identifier: CA2668589021
Gene: SPATA16 HGNC NCBI

Linked Data

gnomAD v4: 3-173019414-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.173019414C>T , CM000665.2:g.173019414C>T GRCh38
NC_000003.11:g.172737204C>T , CM000665.1:g.172737204C>T GRCh37
NC_000003.10:g.174219898C>T NCBI36
NG_021422.1:g.126855G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000351008.4:c.848+72G>A MANE Select ENSP00000341765.3:n.848+72G>A
ENST00000351008.3:c.848+72G>A ENSP00000341765.3:n.848+72G>A
NM_031955.5:c.848+72G>A NP_114161.3:n.848+72G>A
XM_006713778.2:c.848+72G>A XP_006713841.1:n.848+72G>A
XM_011513222.1:c.848+72G>A XP_011511524.1:n.848+72G>A
XM_006713778.3:c.848+72G>A XP_006713841.1:n.848+72G>A
XM_017007308.2:c.848+72G>A XP_016862797.1:n.848+72G>A
NM_031955.6:c.848+72G>A MANE Select NP_114161.3:n.848+72G>A
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