Canonical Allele Identifier: CA635719645
Gene: SNTA1 HGNC NCBI

Linked Data

dbSNP Id: rs1568765314
gnomAD v2: 20-32031528-G-GGCCAGCCGC
gnomAD v3: 20-33443722-G-GGCCAGCCGC
gnomAD v4: 20-33443722-G-GGCCAGCCGC
MyVariant Identifiers: chr20:g.32031528_32031529insGCCAGCCGC (hg19) chr20:g.33443722_33443723insGCCAGCCGC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33443723_33443731dup , CM000682.2:g.33443723_33443731dup GRCh38
NC_000020.10:g.32031529_32031537dup , CM000682.1:g.32031529_32031537dup GRCh37
NC_000020.9:g.31495190_31495198dup NCBI36
NG_011622.1:g.5162_5170dup , LRG_332:g.5162_5170dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.3:c.-111_-103dup MANE Select ENSP00000217381.2:n.-111_-103dup
ENST00000217381.2:c.-111_-103dup ENSP00000217381.2:n.-111_-103dup
NM_003098.2:c.-111_-103dup , LRG_332t1:c.-111_-103dup NP_003089.1:n.-111_-103dup
XM_005260517.1:c.-111_-103dup XP_005260574.1:n.-111_-103dup
XM_011529007.1:c.-111_-103dup XP_011527309.1:n.-111_-103dup
XM_011529008.1:c.-111_-103dup XP_011527310.1:n.-111_-103dup
XR_936612.1:n.123_131dup
NM_003098.3:c.-111_-103dup MANE Select NP_003089.1:n.-111_-103dup
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