Canonical Allele Identifier: CA379924060

Gene: ANO5

Linked Data

• gnomAD v4: 11-22272987-A-G
• MyVariant Identifiers: chr11:g.22294533A>G (hg19) ; chr11:g.22272987A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22272987A>G , CM000673.2:g.22272987A>G	GRCh38
NC_000011.9:g.22294533A>G , CM000673.1:g.22294533A>G	GRCh37
NC_000011.8:g.22251109A>G	NCBI36
NG_015844.1:g.84812A>G , LRG_868:g.84812A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000532043.2:n.250A>G
ENST00000682266.1:c.1783A>G	ENSP00000507766.1:p.Asn595Asp
ENST00000682341.1:c.2191A>G	ENSP00000508251.1:p.Asn731Asp
ENST00000683197.1:c.2191A>G	ENSP00000507641.1:p.Asn731Asp
ENST00000683411.1:c.1783A>G	ENSP00000508397.1:p.Asn595Asp
ENST00000683437.1:c.1783A>G	ENSP00000508408.1:p.Asn595Asp
ENST00000683613.1:n.3227A>G
ENST00000684663.1:c.2188A>G	ENSP00000508009.1:p.Asn730Asp
ENST00000324559.9:c.2233A>G MANE Select	ENSP00000315371.9:p.Asn745Asp
ENST00000648804.1:n.2568A>G
ENST00000324559.8:c.2233A>G	ENSP00000315371.8:p.Asn745Asp
ENST00000532043.1:n.250A>G
NM_001142649.1:c.2230A>G	NP_001136121.1:p.Asn744Asp
NM_213599.2:c.2233A>G , LRG_868t1:c.2233A>G	NP_998764.1:p.Asn745Asp
XM_005252820.2:c.2191A>G	XP_005252877.2:p.Asn731Asp
XM_005252821.2:c.2188A>G	XP_005252878.2:p.Asn730Asp
XM_005252822.3:c.2155A>G	XP_005252879.1:p.Asn719Asp
XM_005252823.3:c.2152A>G	XP_005252880.1:p.Asn718Asp
XM_011519949.1:c.2140A>G	XP_011518251.1:p.Asn714Asp
XM_005252820.3:c.2191A>G	XP_005252877.2:p.Asn731Asp
XM_005252821.3:c.2188A>G	XP_005252878.2:p.Asn730Asp
XM_005252822.4:c.2155A>G	XP_005252879.1:p.Asn719Asp
XM_011519949.2:c.2140A>G	XP_011518251.1:p.Asn714Asp
NM_001142649.2:c.2230A>G	NP_001136121.1:p.Asn744Asp
NM_213599.3:c.2233A>G MANE Select	NP_998764.1:p.Asn745Asp