Canonical Allele Identifier: CA11729673
Gene: SMARCAD1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs11097407

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.94224984G>C , CM000666.2:g.94224984G>C GRCh38
NC_000004.11:g.95146135G>C , CM000666.1:g.95146135G>C GRCh37
NC_000004.10:g.95365158G>C NCBI36
NG_031945.1:g.22377G>C

Transcript Alleles

HGVS Amino-acid change
NM_001128429.2:c.191-1135G>C VV NP_001121901.1:p.=
NM_001128430.1:c.191-1135G>C VV NP_001121902.1:p.=
NM_020159.4:c.191-1135G>C VV NP_064544.2:p.=
NR_045644.1:n.517-1135G>C
XR_938765.1:n.446-1135G>C
XR_938766.1:n.446-1135G>C
XM_017008463.2:c.191-1135G>C XP_016863952.1:p.=
XM_017008464.2:c.-1556-1135G>C XP_016863953.1:p.=
XM_017008465.2:c.-1556-1135G>C XP_016863954.1:p.=
XM_024454154.1:c.191-1135G>C XP_024309922.1:p.=
XR_001741292.2:n.368-1135G>C
XR_938765.2:n.446-1135G>C
ENST00000354268.8:c.191-1135G>C ENSP00000346217.4:p.=
ENST00000359052.8:c.191-1135G>C ENSP00000351947.4:p.=
ENST00000394961.6:c.*96-1135G>C ENSP00000378413.2:p.=
ENST00000457823.6:c.191-1135G>C ENSP00000415576.2:p.=
ENST00000510105.5:c.191-1135G>C ENSP00000424624.1:p.=