Canonical Allele Identifier: CA431403423

Gene: SMARCAL1

Linked Data

• MyVariant Identifiers: chr2:g.217347640A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.216482917A>C , CM000664.2:g.216482917A>C	GRCh38
NC_000002.11:g.217347640A>C , CM000664.1:g.217347640A>C	GRCh37
NC_000002.10:g.217055885A>C	NCBI36
NG_009771.1:g.75504A>C , LRG_108:g.75504A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000425815.6:c.2805A>C	ENSP00000394410.2:p.Pro935=
ENST00000430374.6:c.2805A>C	ENSP00000405077.2:p.Pro935=
ENST00000444508.6:c.2805A>C	ENSP00000398969.2:p.Pro935=
ENST00000697899.1:c.2571A>C	ENSP00000513470.1:p.Pro857=
ENST00000697901.1:c.*1560A>C	ENSP00000513471.1:n.*1560A>C
ENST00000697903.1:c.*1292A>C	ENSP00000513472.1:n.*1292A>C
ENST00000697904.1:c.*1292A>C	ENSP00000513473.1:n.*1292A>C
ENST00000697905.1:c.*1292A>C	ENSP00000513474.1:n.*1292A>C
ENST00000697906.1:c.2571A>C	ENSP00000513475.1:p.Pro857=
ENST00000697907.1:c.*1663A>C	ENSP00000513476.1:n.*1663A>C
ENST00000697909.1:n.1697A>C
ENST00000697910.1:n.1202A>C
ENST00000357276.9:c.2805A>C MANE Select	ENSP00000349823.4:p.Pro935=
ENST00000357276.8:c.2805A>C	ENSP00000349823.4:p.Pro935=
ENST00000358207.9:c.2805A>C	ENSP00000350940.5:p.Pro935=
ENST00000392128.6:c.2331A>C	ENSP00000375974.2:p.Pro777=
NM_001127207.1:c.2805A>C	NP_001120679.1:p.Pro935=
NM_014140.3:c.2805A>C , LRG_108t1:c.2805A>C	NP_054859.2:p.Pro935=
XM_005246631.2:c.2805A>C	XP_005246688.1:p.Pro935=
XM_005246632.1:c.2805A>C	XP_005246689.1:p.Pro935=
XM_006712557.1:c.2739A>C	XP_006712620.1:p.Pro913=
XM_005246632.2:c.2805A>C	XP_005246689.1:p.Pro935=
XM_017004228.2:c.1893A>C	XP_016859717.1:p.Pro631=
NM_001127207.2:c.2805A>C	NP_001120679.1:p.Pro935=
NM_014140.4:c.2805A>C MANE Select	NP_054859.2:p.Pro935=