Canonical Allele Identifier: CA2580810748

Gene: TEX15

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.30845915T= , CM000670.2:g.30845915T=	GRCh38
NC_000008.10:g.30703431T= , CM000670.1:g.30703431T=	GRCh37
NC_000008.9:g.30822973T=	NCBI36
NG_053141.1:g.72098A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256246.5:c.3103A=	ENSP00000256246.2:p.Ile1035=
ENST00000638951.1:c.4264A=	ENSP00000492713.1:p.Ile1422=
ENST00000643185.2:c.4252A= MANE Select	ENSP00000493555.1:p.Ile1418=
ENST00000256246.4:c.3103A=	ENSP00000256246.2:p.Ile1035=
NM_031271.3:c.3103A=	NP_112561.2:p.Ile1035=
XM_005273575.2:c.4252A=	XP_005273632.1:p.Ile1418=
XM_005273576.2:c.3943A=	XP_005273633.1:p.Ile1315=
XM_006716369.2:c.4252A=	XP_006716432.1:p.Ile1418=
XM_011544588.1:c.4264A=	XP_011542890.1:p.Ile1422=
XM_011544589.1:c.4252A=	XP_011542891.1:p.Ile1418=
XM_011544590.1:c.4252A=	XP_011542892.1:p.Ile1418=
XM_011544591.1:c.4252A=	XP_011542893.1:p.Ile1418=
XM_011544592.1:c.4252A=	XP_011542894.1:p.Ile1418=
XM_011544593.1:c.3943A=	XP_011542895.1:p.Ile1315=
XM_011544594.1:c.4264A=	XP_011542896.1:p.Ile1422=
NM_001350162.1:c.4252A=	NP_001337091.1:p.Ile1418=
XM_006716369.4:c.4252A=	XP_006716432.1:p.Ile1418=
XM_011544588.2:c.4264A=	XP_011542890.1:p.Ile1422=
XM_011544589.3:c.4252A=	XP_011542891.1:p.Ile1418=
XM_011544590.3:c.4252A=	XP_011542892.1:p.Ile1418=
XM_011544591.3:c.4252A=	XP_011542893.1:p.Ile1418=
XM_011544592.3:c.4252A=	XP_011542894.1:p.Ile1418=
XM_011544593.3:c.3943A=	XP_011542895.1:p.Ile1315=
XM_011544594.2:c.4264A=	XP_011542896.1:p.Ile1422=
XM_024447196.1:c.4252A=	XP_024302964.1:p.Ile1418=
XM_024447197.1:c.3943A=	XP_024302965.1:p.Ile1315=
NM_001350162.2:c.4252A= MANE Select	NP_001337091.1:p.Ile1418=