Canonical Allele Identifier: CA548089177
Gene: SPATA16 HGNC NCBI

Linked Data

dbSNP Id: rs1204815357

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.173081062G>C , CM000665.2:g.173081062G>C GRCh38
NC_000003.11:g.172798852G>C , CM000665.1:g.172798852G>C GRCh37
NC_000003.10:g.174281546G>C NCBI36
NG_021422.1:g.65207C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000351008.4:c.613-31968C>G MANE Select ENSP00000341765.3:n.613-31968C>G
ENST00000351008.3:c.613-31968C>G ENSP00000341765.3:n.613-31968C>G
NM_031955.5:c.613-31968C>G NP_114161.3:n.613-31968C>G
XM_006713778.2:c.613-31968C>G XP_006713841.1:n.613-31968C>G
XM_011513222.1:c.613-31968C>G XP_011511524.1:n.613-31968C>G
XM_006713778.3:c.613-31968C>G XP_006713841.1:n.613-31968C>G
XM_017007308.2:c.613-31968C>G XP_016862797.1:n.613-31968C>G
NM_031955.6:c.613-31968C>G MANE Select NP_114161.3:n.613-31968C>G