Canonical Allele Identifier: CA431403196

Gene: SMARCAL1

Linked Data

• MyVariant Identifiers: chr2:g.217347758A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.216483035A>C , CM000664.2:g.216483035A>C	GRCh38
NC_000002.11:g.217347758A>C , CM000664.1:g.217347758A>C	GRCh37
NC_000002.10:g.217056003A>C	NCBI36
NG_009771.1:g.75622A>C , LRG_108:g.75622A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000425815.6:c.*58A>C	ENSP00000394410.2:n.*58A>C
ENST00000430374.6:c.*58A>C	ENSP00000405077.2:n.*58A>C
ENST00000444508.6:c.*58A>C	ENSP00000398969.2:n.*58A>C
ENST00000697899.1:c.*58A>C	ENSP00000513470.1:n.*58A>C
ENST00000697907.1:c.*1781A>C	ENSP00000513476.1:n.*1781A>C
ENST00000357276.9:c.*58A>C MANE Select	ENSP00000349823.4:n.*58A>C
ENST00000357276.8:c.*58A>C	ENSP00000349823.4:n.*58A>C
NM_001127207.1:c.*58A>C	NP_001120679.1:n.*58A>C
NM_014140.3:c.*58A>C , LRG_108t1:c.*58A>C	NP_054859.2:n.*58A>C
XM_005246631.2:c.*58A>C	XP_005246688.1:n.*58A>C
XM_005246632.1:c.*58A>C	XP_005246689.1:n.*58A>C
XM_006712557.1:c.*58A>C	XP_006712620.1:n.*58A>C
XM_005246632.2:c.*58A>C	XP_005246689.1:n.*58A>C
XM_017004228.2:c.*58A>C	XP_016859717.1:n.*58A>C
NM_001127207.2:c.*58A>C	NP_001120679.1:n.*58A>C
NM_014140.4:c.*58A>C MANE Select	NP_054859.2:n.*58A>C