Canonical Allele Identifier: CA292951500
Gene: SMARCD2 HGNC NCBI

Linked Data

dbSNP Id: rs35239390
MyVariant Identifiers: chr17:g.61909446_61909447insC (hg19) chr17:g.63832086_63832087insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63832086_63832087insC , CM000679.2:g.63832086_63832087insC GRCh38
NC_000017.10:g.61909446_61909447insC , CM000679.1:g.61909446_61909447insC GRCh37
NC_000017.9:g.59263178_59263179insC NCBI36
NG_053004.1:g.15905_15906insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000448276.7:c.*851_*852insG MANE Select ENSP00000392617.2:n.*851_*852insG
ENST00000448276.6:c.*851_*852insG ENSP00000392617.2:n.*851_*852insG
ENST00000613943.4:c.2336_2337insG ENSP00000483605.1:n.2336_2337insG
NM_001098426.1:c.*851_*852insG NP_001091896.1:n.*851_*852insG
XM_005257604.2:c.*851_*852insG XP_005257661.2:n.*851_*852insG
NM_001330439.1:c.*851_*852insG NP_001317368.1:n.*851_*852insG
NM_001330440.1:c.*851_*852insG NP_001317369.1:n.*851_*852insG
NM_001098426.2:c.*851_*852insG MANE Select NP_001091896.1:n.*851_*852insG
NM_001330440.2:c.*851_*852insG NP_001317369.1:n.*851_*852insG
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