Canonical Allele Identifier: CA1327851093

Gene: SMARCAL1

Linked Data

• dbSNP Id: rs1695234433
• gnomAD v4: 2-216483024-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.216483024T>C , CM000664.2:g.216483024T>C	GRCh38
NC_000002.11:g.217347747T>C , CM000664.1:g.217347747T>C	GRCh37
NC_000002.10:g.217055992T>C	NCBI36
NG_009771.1:g.75611T>C , LRG_108:g.75611T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000425815.6:c.*47T>C	ENSP00000394410.2:n.*47T>C
ENST00000430374.6:c.*47T>C	ENSP00000405077.2:n.*47T>C
ENST00000444508.6:c.*47T>C	ENSP00000398969.2:n.*47T>C
ENST00000697899.1:c.*47T>C	ENSP00000513470.1:n.*47T>C
ENST00000697903.1:c.*1399T>C	ENSP00000513472.1:n.*1399T>C
ENST00000697904.1:c.*1399T>C	ENSP00000513473.1:n.*1399T>C
ENST00000697905.1:c.*1399T>C	ENSP00000513474.1:n.*1399T>C
ENST00000697906.1:c.*47T>C	ENSP00000513475.1:n.*47T>C
ENST00000697907.1:c.*1770T>C	ENSP00000513476.1:n.*1770T>C
ENST00000697909.1:n.1804T>C
ENST00000697910.1:n.1309T>C
ENST00000357276.9:c.*47T>C MANE Select	ENSP00000349823.4:n.*47T>C
ENST00000357276.8:c.*47T>C	ENSP00000349823.4:n.*47T>C
NM_001127207.1:c.*47T>C	NP_001120679.1:n.*47T>C
NM_014140.3:c.*47T>C , LRG_108t1:c.*47T>C	NP_054859.2:n.*47T>C
XM_005246631.2:c.*47T>C	XP_005246688.1:n.*47T>C
XM_005246632.1:c.*47T>C	XP_005246689.1:n.*47T>C
XM_006712557.1:c.*47T>C	XP_006712620.1:n.*47T>C
XM_005246632.2:c.*47T>C	XP_005246689.1:n.*47T>C
XM_017004228.2:c.*47T>C	XP_016859717.1:n.*47T>C
NM_001127207.2:c.*47T>C	NP_001120679.1:n.*47T>C
NM_014140.4:c.*47T>C MANE Select	NP_054859.2:n.*47T>C