Canonical Allele Identifier: CA1957403092

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22272942_22272943delinsTG , CM000673.2:g.22272942_22272943delinsTG	GRCh38
NC_000011.9:g.22294488_22294489delinsTG , CM000673.1:g.22294488_22294489delinsTG	GRCh37
NC_000011.8:g.22251064_22251065delinsTG	NCBI36
NG_015844.1:g.84767_84768delinsTG , LRG_868:g.84767_84768delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000532043.2:n.205_206delinsTG
ENST00000682266.1:c.1738_1739delinsTG	ENSP00000507766.1:p.Trp580=
ENST00000682341.1:c.2146_2147delinsTG	ENSP00000508251.1:p.Trp716=
ENST00000683197.1:c.2146_2147delinsTG	ENSP00000507641.1:p.Trp716=
ENST00000683411.1:c.1738_1739delinsTG	ENSP00000508397.1:p.Trp580=
ENST00000683437.1:c.1738_1739delinsTG	ENSP00000508408.1:p.Trp580=
ENST00000683613.1:n.3182_3183delinsTG
ENST00000684663.1:c.2143_2144delinsTG	ENSP00000508009.1:p.Trp715=
ENST00000324559.9:c.2188_2189delinsTG MANE Select	ENSP00000315371.9:p.Trp730=
ENST00000648804.1:n.2523_2524delinsTG
ENST00000324559.8:c.2188_2189delinsTG	ENSP00000315371.8:p.Trp730=
ENST00000532043.1:n.205_206delinsTG
NM_001142649.1:c.2185_2186delinsTG	NP_001136121.1:p.Trp729=
NM_213599.2:c.2188_2189delinsTG , LRG_868t1:c.2188_2189delinsTG	NP_998764.1:p.Trp730=
XM_005252820.2:c.2146_2147delinsTG	XP_005252877.2:p.Trp716=
XM_005252821.2:c.2143_2144delinsTG	XP_005252878.2:p.Trp715=
XM_005252822.3:c.2110_2111delinsTG	XP_005252879.1:p.Trp704=
XM_005252823.3:c.2107_2108delinsTG	XP_005252880.1:p.Trp703=
XM_011519949.1:c.2095_2096delinsTG	XP_011518251.1:p.Trp699=
XM_005252820.3:c.2146_2147delinsTG	XP_005252877.2:p.Trp716=
XM_005252821.3:c.2143_2144delinsTG	XP_005252878.2:p.Trp715=
XM_005252822.4:c.2110_2111delinsTG	XP_005252879.1:p.Trp704=
XM_011519949.2:c.2095_2096delinsTG	XP_011518251.1:p.Trp699=
NM_001142649.2:c.2185_2186delinsTG	NP_001136121.1:p.Trp729=
NM_213599.3:c.2188_2189delinsTG MANE Select	NP_998764.1:p.Trp730=