Canonical Allele Identifier: CA379923977

Gene: ANO5

Linked Data

• MyVariant Identifiers: chr11:g.22294494G>T (hg19) ; chr11:g.22272948G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22272948G>T , CM000673.2:g.22272948G>T	GRCh38
NC_000011.9:g.22294494G>T , CM000673.1:g.22294494G>T	GRCh37
NC_000011.8:g.22251070G>T	NCBI36
NG_015844.1:g.84773G>T , LRG_868:g.84773G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000532043.2:n.211G>T
ENST00000682266.1:c.1744G>T	ENSP00000507766.1:p.Asp582Tyr
ENST00000682341.1:c.2152G>T	ENSP00000508251.1:p.Asp718Tyr
ENST00000683197.1:c.2152G>T	ENSP00000507641.1:p.Asp718Tyr
ENST00000683411.1:c.1744G>T	ENSP00000508397.1:p.Asp582Tyr
ENST00000683437.1:c.1744G>T	ENSP00000508408.1:p.Asp582Tyr
ENST00000683613.1:n.3188G>T
ENST00000684663.1:c.2149G>T	ENSP00000508009.1:p.Asp717Tyr
ENST00000324559.9:c.2194G>T MANE Select	ENSP00000315371.9:p.Asp732Tyr
ENST00000648804.1:n.2529G>T
ENST00000324559.8:c.2194G>T	ENSP00000315371.8:p.Asp732Tyr
ENST00000532043.1:n.211G>T
NM_001142649.1:c.2191G>T	NP_001136121.1:p.Asp731Tyr
NM_213599.2:c.2194G>T , LRG_868t1:c.2194G>T	NP_998764.1:p.Asp732Tyr
XM_005252820.2:c.2152G>T	XP_005252877.2:p.Asp718Tyr
XM_005252821.2:c.2149G>T	XP_005252878.2:p.Asp717Tyr
XM_005252822.3:c.2116G>T	XP_005252879.1:p.Asp706Tyr
XM_005252823.3:c.2113G>T	XP_005252880.1:p.Asp705Tyr
XM_011519949.1:c.2101G>T	XP_011518251.1:p.Asp701Tyr
XM_005252820.3:c.2152G>T	XP_005252877.2:p.Asp718Tyr
XM_005252821.3:c.2149G>T	XP_005252878.2:p.Asp717Tyr
XM_005252822.4:c.2116G>T	XP_005252879.1:p.Asp706Tyr
XM_011519949.2:c.2101G>T	XP_011518251.1:p.Asp701Tyr
NM_001142649.2:c.2191G>T	NP_001136121.1:p.Asp731Tyr
NM_213599.3:c.2194G>T MANE Select	NP_998764.1:p.Asp732Tyr