Canonical Allele Identifier: CA379923688

Gene: ANO5

Linked Data

• MyVariant Identifiers: chr11:g.22294372C>T (hg19) ; chr11:g.22272826C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22272826C>T , CM000673.2:g.22272826C>T	GRCh38
NC_000011.9:g.22294372C>T , CM000673.1:g.22294372C>T	GRCh37
NC_000011.8:g.22250948C>T	NCBI36
NG_015844.1:g.84651C>T , LRG_868:g.84651C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000532043.2:n.89C>T
ENST00000682266.1:c.1622C>T	ENSP00000507766.1:p.Pro541Leu
ENST00000682341.1:c.2030C>T	ENSP00000508251.1:p.Pro677Leu
ENST00000683197.1:c.2030C>T	ENSP00000507641.1:p.Pro677Leu
ENST00000683411.1:c.1622C>T	ENSP00000508397.1:p.Pro541Leu
ENST00000683437.1:c.1622C>T	ENSP00000508408.1:p.Pro541Leu
ENST00000683613.1:n.3066C>T
ENST00000684663.1:c.2027C>T	ENSP00000508009.1:p.Pro676Leu
ENST00000324559.9:c.2072C>T MANE Select	ENSP00000315371.9:p.Pro691Leu
ENST00000648804.1:n.2407C>T
ENST00000324559.8:c.2072C>T	ENSP00000315371.8:p.Pro691Leu
ENST00000532043.1:n.89C>T
NM_001142649.1:c.2069C>T	NP_001136121.1:p.Pro690Leu
NM_213599.2:c.2072C>T , LRG_868t1:c.2072C>T	NP_998764.1:p.Pro691Leu
XM_005252820.2:c.2030C>T	XP_005252877.2:p.Pro677Leu
XM_005252821.2:c.2027C>T	XP_005252878.2:p.Pro676Leu
XM_005252822.3:c.1994C>T	XP_005252879.1:p.Pro665Leu
XM_005252823.3:c.1991C>T	XP_005252880.1:p.Pro664Leu
XM_011519949.1:c.1979C>T	XP_011518251.1:p.Pro660Leu
XM_005252820.3:c.2030C>T	XP_005252877.2:p.Pro677Leu
XM_005252821.3:c.2027C>T	XP_005252878.2:p.Pro676Leu
XM_005252822.4:c.1994C>T	XP_005252879.1:p.Pro665Leu
XM_011519949.2:c.1979C>T	XP_011518251.1:p.Pro660Leu
NM_001142649.2:c.2069C>T	NP_001136121.1:p.Pro690Leu
NM_213599.3:c.2072C>T MANE Select	NP_998764.1:p.Pro691Leu