Canonical Allele Identifier: CA361136443

Gene: SIL1

Linked Data

• MyVariant Identifiers: chr5:g.138282867T>G (hg19) ; chr5:g.138947178T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.138947178T>G , CM000667.2:g.138947178T>G	GRCh38
NC_000005.9:g.138282867T>G , CM000667.1:g.138282867T>G	GRCh37
NC_000005.8:g.138310766T>G	NCBI36
NG_008112.1:g.256199A>C
NG_008112.2:g.256199A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394817.7:c.1325A>C MANE Select	ENSP00000378294.2:p.Asp442Ala
ENST00000265195.9:c.1325A>C	ENSP00000265195.5:p.Asp442Ala
ENST00000394817.6:c.1325A>C	ENSP00000378294.2:p.Asp442Ala
ENST00000509534.5:c.1346A>C	ENSP00000426858.1:p.Asp449Ala
ENST00000515008.1:n.660A>C
NM_001037633.1:c.1325A>C	NP_001032722.1:p.Asp442Ala
NM_022464.4:c.1325A>C	NP_071909.1:p.Asp442Ala
XM_011543570.1:c.1355A>C	XP_011541872.1:p.Asp452Ala
XM_011543570.2:c.1355A>C	XP_011541872.1:p.Asp452Ala
XM_024446164.1:c.1325A>C	XP_024301932.1:p.Asp442Ala
NM_022464.5:c.1325A>C MANE Select	NP_071909.1:p.Asp442Ala
NM_001037633.2:c.1325A>C	NP_001032722.1:p.Asp442Ala