Canonical Allele Identifier: CA361136616

Gene: SIL1

Linked Data

• MyVariant Identifiers: chr5:g.138282951T>A (hg19) ; chr5:g.138947262T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.138947262T>A , CM000667.2:g.138947262T>A	GRCh38
NC_000005.9:g.138282951T>A , CM000667.1:g.138282951T>A	GRCh37
NC_000005.8:g.138310850T>A	NCBI36
NG_008112.1:g.256115A>T
NG_008112.2:g.256115A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394817.7:c.1241A>T MANE Select	ENSP00000378294.2:p.Gln414Leu
ENST00000265195.9:c.1241A>T	ENSP00000265195.5:p.Gln414Leu
ENST00000394817.6:c.1241A>T	ENSP00000378294.2:p.Gln414Leu
ENST00000509534.5:c.1262A>T	ENSP00000426858.1:p.Gln421Leu
ENST00000515008.1:n.576A>T
NM_001037633.1:c.1241A>T	NP_001032722.1:p.Gln414Leu
NM_022464.4:c.1241A>T	NP_071909.1:p.Gln414Leu
XM_011543570.1:c.1271A>T	XP_011541872.1:p.Gln424Leu
XM_011543570.2:c.1271A>T	XP_011541872.1:p.Gln424Leu
XM_024446164.1:c.1241A>T	XP_024301932.1:p.Gln414Leu
NM_022464.5:c.1241A>T MANE Select	NP_071909.1:p.Gln414Leu
NM_001037633.2:c.1241A>T	NP_001032722.1:p.Gln414Leu