Canonical Allele Identifier: CA1420795408
Gene: SPATA16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.173081067_173081068delinsGT , CM000665.2:g.173081067_173081068delinsGT GRCh38
NC_000003.11:g.172798857_172798858delinsGT , CM000665.1:g.172798857_172798858delinsGT GRCh37
NC_000003.10:g.174281551_174281552delinsGT NCBI36
NG_021422.1:g.65201_65202delinsAC

Transcript Alleles

HGVS Amino-acid change
ENST00000351008.4:c.613-31974_613-31973delinsAC MANE Select ENSP00000341765.3:n.613-31974_613-31973de...
ENST00000351008.3:c.613-31974_613-31973delinsAC ENSP00000341765.3:n.613-31974_613-31973de...
NM_031955.5:c.613-31974_613-31973delinsAC NP_114161.3:n.613-31974_613-31973delinsAC...
XM_006713778.2:c.613-31974_613-31973delinsAC XP_006713841.1:n.613-31974_613-31973delin...
XM_011513222.1:c.613-31974_613-31973delinsAC XP_011511524.1:n.613-31974_613-31973delin...
XM_006713778.3:c.613-31974_613-31973delinsAC XP_006713841.1:n.613-31974_613-31973delin...
XM_017007308.2:c.613-31974_613-31973delinsAC XP_016862797.1:n.613-31974_613-31973delin...
NM_031955.6:c.613-31974_613-31973delinsAC MANE Select NP_114161.3:n.613-31974_613-31973delinsAC...