Canonical Allele Identifier: CA2645527094

Gene: STIL

Linked Data

• gnomAD v4: 1-47262825-AAC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.47262826_47262827del , CM000663.2:g.47262826_47262827del	GRCh38
NC_000001.10:g.47728498_47728499del , CM000663.1:g.47728498_47728499del	GRCh37
NC_000001.9:g.47501085_47501086del	NCBI36
NG_012126.1:g.56321_56322del

Transcript Alleles

HGVS	Amino-acid change
ENST00000337817.10:c.2688+76_2688+77del	ENSP00000337367.6:n.2688+76_2688+77del
ENST00000447475.7:c.2634+76_2634+77del	ENSP00000411664.3:n.2634+76_2634+77del
ENST00000682940.1:n.1379+76_1379+77del
ENST00000682977.1:c.2688+76_2688+77del	ENSP00000506981.1:n.2688+76_2688+77del
ENST00000683977.1:c.2125+76_2125+77del
ENST00000684618.1:n.1601+76_1601+77del
ENST00000371877.8:c.2829+76_2829+77del MANE Select	ENSP00000360944.3:n.2829+76_2829+77del
ENST00000337817.9:c.2688+76_2688+77del	ENSP00000337367.6:n.2688+76_2688+77del
ENST00000360380.7:c.2826+76_2826+77del	ENSP00000353544.3:n.2826+76_2826+77del
ENST00000371877.7:c.2829+76_2829+77del	ENSP00000360944.3:n.2829+76_2829+77del
ENST00000396221.6:c.2775+76_2775+77del	ENSP00000379523.2:n.2775+76_2775+77del
ENST00000418131.1:n.3307+76_3307+77del
ENST00000447475.6:c.2634+76_2634+77del	ENSP00000411664.2:n.2634+76_2634+77del
NM_001048166.1:c.2829+76_2829+77del MANE Select	NP_001041631.1:n.2829+76_2829+77del
NM_001282936.1:c.2826+76_2826+77del	NP_001269865.1:n.2826+76_2826+77del
NM_001282937.1:c.2775+76_2775+77del	NP_001269866.1:n.2775+76_2775+77del
NM_001282938.1:c.2688+76_2688+77del	NP_001269867.1:n.2688+76_2688+77del
NM_001282939.1:c.2634+76_2634+77del	NP_001269868.1:n.2634+76_2634+77del
NM_003035.2:c.2826+76_2826+77del	NP_003026.2:n.2826+76_2826+77del
XM_006710834.2:c.2829+76_2829+77del	XP_006710897.1:n.2829+76_2829+77del
XM_011541991.1:c.2829+76_2829+77del	XP_011540293.1:n.2829+76_2829+77del
XM_011541992.1:c.2829+76_2829+77del	XP_011540294.1:n.2829+76_2829+77del
XM_011541993.1:c.2826+76_2826+77del	XP_011540295.1:n.2826+76_2826+77del
XM_011541994.1:c.2775+76_2775+77del	XP_011540296.1:n.2775+76_2775+77del
XM_011541995.1:c.2775+76_2775+77del	XP_011540297.1:n.2775+76_2775+77del
XM_011541996.1:c.2688+76_2688+77del	XP_011540298.1:n.2688+76_2688+77del
XM_011541997.1:c.2688+76_2688+77del	XP_011540299.1:n.2688+76_2688+77del
XM_011541998.1:c.2634+76_2634+77del	XP_011540300.1:n.2634+76_2634+77del
XM_011541999.1:c.2133+76_2133+77del	XP_011540301.1:n.2133+76_2133+77del
XM_011542000.1:c.2133+76_2133+77del	XP_011540302.1:n.2133+76_2133+77del
XM_011542001.1:c.2829+76_2829+77del	XP_011540303.1:n.2829+76_2829+77del
XM_006710834.3:c.2829+76_2829+77del	XP_006710897.1:n.2829+76_2829+77del
XM_011541991.2:c.2829+76_2829+77del	XP_011540293.1:n.2829+76_2829+77del
XM_011541992.2:c.2829+76_2829+77del	XP_011540294.1:n.2829+76_2829+77del
XM_011541994.2:c.2775+76_2775+77del	XP_011540296.1:n.2775+76_2775+77del
XM_011541996.2:c.2688+76_2688+77del	XP_011540298.1:n.2688+76_2688+77del
XM_011541998.2:c.2634+76_2634+77del	XP_011540300.1:n.2634+76_2634+77del
XM_011542001.2:c.2829+76_2829+77del	XP_011540303.1:n.2829+76_2829+77del
XM_017002123.1:c.2685+76_2685+77del	XP_016857612.1:n.2685+76_2685+77del
XM_017002124.1:c.2118+76_2118+77del	XP_016857613.1:n.2118+76_2118+77del
XM_017002125.1:c.2826+76_2826+77del	XP_016857614.1:n.2826+76_2826+77del
XM_017002126.1:c.2775+76_2775+77del	XP_016857615.1:n.2775+76_2775+77del
XR_001737370.1:n.2981+76_2981+77del
NM_001377417.1:c.2688+76_2688+77del	NP_001364346.1:n.2688+76_2688+77del