Canonical Allele Identifier: CA379923989

Gene: ANO5

Linked Data

• MyVariant Identifiers: chr11:g.22294499T>G (hg19) ; chr11:g.22272953T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22272953T>G , CM000673.2:g.22272953T>G	GRCh38
NC_000011.9:g.22294499T>G , CM000673.1:g.22294499T>G	GRCh37
NC_000011.8:g.22251075T>G	NCBI36
NG_015844.1:g.84778T>G , LRG_868:g.84778T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000532043.2:n.216T>G
ENST00000682266.1:c.1749T>G	ENSP00000507766.1:p.Ile583Met
ENST00000682341.1:c.2157T>G	ENSP00000508251.1:p.Ile719Met
ENST00000683197.1:c.2157T>G	ENSP00000507641.1:p.Ile719Met
ENST00000683411.1:c.1749T>G	ENSP00000508397.1:p.Ile583Met
ENST00000683437.1:c.1749T>G	ENSP00000508408.1:p.Ile583Met
ENST00000683613.1:n.3193T>G
ENST00000684663.1:c.2154T>G	ENSP00000508009.1:p.Ile718Met
ENST00000324559.9:c.2199T>G MANE Select	ENSP00000315371.9:p.Ile733Met
ENST00000648804.1:n.2534T>G
ENST00000324559.8:c.2199T>G	ENSP00000315371.8:p.Ile733Met
ENST00000532043.1:n.216T>G
NM_001142649.1:c.2196T>G	NP_001136121.1:p.Ile732Met
NM_213599.2:c.2199T>G , LRG_868t1:c.2199T>G	NP_998764.1:p.Ile733Met
XM_005252820.2:c.2157T>G	XP_005252877.2:p.Ile719Met
XM_005252821.2:c.2154T>G	XP_005252878.2:p.Ile718Met
XM_005252822.3:c.2121T>G	XP_005252879.1:p.Ile707Met
XM_005252823.3:c.2118T>G	XP_005252880.1:p.Ile706Met
XM_011519949.1:c.2106T>G	XP_011518251.1:p.Ile702Met
XM_005252820.3:c.2157T>G	XP_005252877.2:p.Ile719Met
XM_005252821.3:c.2154T>G	XP_005252878.2:p.Ile718Met
XM_005252822.4:c.2121T>G	XP_005252879.1:p.Ile707Met
XM_011519949.2:c.2106T>G	XP_011518251.1:p.Ile702Met
NM_001142649.2:c.2196T>G	NP_001136121.1:p.Ile732Met
NM_213599.3:c.2199T>G MANE Select	NP_998764.1:p.Ile733Met