Canonical Allele Identifier: CA340235964

Gene: STIL

Linked Data

• MyVariant Identifiers: chr1:g.47725974C>G (hg19) ; chr1:g.47260302C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.47260302C>G , CM000663.2:g.47260302C>G	GRCh38
NC_000001.10:g.47725974C>G , CM000663.1:g.47725974C>G	GRCh37
NC_000001.9:g.47498561C>G	NCBI36
NG_012126.1:g.58846G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337817.10:c.2926G>C	ENSP00000337367.6:p.Val976Leu
ENST00000447475.7:c.2872G>C	ENSP00000411664.3:p.Val958Leu
ENST00000682940.1:n.1617G>C
ENST00000682977.1:c.2926G>C	ENSP00000506981.1:p.Val976Leu
ENST00000683977.1:c.2125+2601G>C
ENST00000684618.1:n.1839G>C
ENST00000371877.8:c.3067G>C MANE Select	ENSP00000360944.3:p.Val1023Leu
ENST00000337817.9:c.2926G>C	ENSP00000337367.6:p.Val976Leu
ENST00000360380.7:c.3064G>C	ENSP00000353544.3:p.Val1022Leu
ENST00000371877.7:c.3067G>C	ENSP00000360944.3:p.Val1023Leu
ENST00000396221.6:c.3013G>C	ENSP00000379523.2:p.Val1005Leu
NM_001048166.1:c.3067G>C MANE Select	NP_001041631.1:p.Val1023Leu
NM_001282936.1:c.3064G>C	NP_001269865.1:p.Val1022Leu
NM_001282937.1:c.3013G>C	NP_001269866.1:p.Val1005Leu
NM_001282938.1:c.2926G>C	NP_001269867.1:p.Val976Leu
NM_001282939.1:c.2872G>C	NP_001269868.1:p.Val958Leu
NM_003035.2:c.3064G>C	NP_003026.2:p.Val1022Leu
XM_006710834.2:c.3067G>C	XP_006710897.1:p.Val1023Leu
XM_011541991.1:c.3067G>C	XP_011540293.1:p.Val1023Leu
XM_011541992.1:c.3067G>C	XP_011540294.1:p.Val1023Leu
XM_011541993.1:c.3064G>C	XP_011540295.1:p.Val1022Leu
XM_011541994.1:c.3013G>C	XP_011540296.1:p.Val1005Leu
XM_011541995.1:c.3013G>C	XP_011540297.1:p.Val1005Leu
XM_011541996.1:c.2926G>C	XP_011540298.1:p.Val976Leu
XM_011541997.1:c.2926G>C	XP_011540299.1:p.Val976Leu
XM_011541998.1:c.2872G>C	XP_011540300.1:p.Val958Leu
XM_011541999.1:c.2371G>C	XP_011540301.1:p.Val791Leu
XM_011542000.1:c.2371G>C	XP_011540302.1:p.Val791Leu
XM_011542001.1:c.2829+2601G>C	XP_011540303.1:n.2829+2601G>C
XM_006710834.3:c.3067G>C	XP_006710897.1:p.Val1023Leu
XM_011541991.2:c.3067G>C	XP_011540293.1:p.Val1023Leu
XM_011541992.2:c.3067G>C	XP_011540294.1:p.Val1023Leu
XM_011541994.2:c.3013G>C	XP_011540296.1:p.Val1005Leu
XM_011541996.2:c.2926G>C	XP_011540298.1:p.Val976Leu
XM_011541998.2:c.2872G>C	XP_011540300.1:p.Val958Leu
XM_011542001.2:c.2829+2601G>C	XP_011540303.1:n.2829+2601G>C
XM_017002123.1:c.2923G>C	XP_016857612.1:p.Val975Leu
XM_017002124.1:c.2356G>C	XP_016857613.1:p.Val786Leu
XM_017002125.1:c.2826+2601G>C	XP_016857614.1:n.2826+2601G>C
XM_017002126.1:c.2775+2601G>C	XP_016857615.1:n.2775+2601G>C
XR_001737370.1:n.3341G>C
NM_001377417.1:c.2926G>C	NP_001364346.1:p.Val976Leu