Canonical Allele Identifier: CA9032259

Gene: CNN2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1037725C>T , CM000681.2:g.1037725C>T	GRCh38
NC_000019.9:g.1037724C>T , CM000681.1:g.1037724C>T	GRCh37
NC_000019.8:g.988724C>T	NCBI36
NG_046909.1:g.2623C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263097.9:c.755C>T MANE Select	ENSP00000263097.2:p.Thr252Met
ENST00000568865.3:c.*91C>T	ENSP00000458137.2:n.*91C>T
ENST00000263097.8:c.755C>T	ENSP00000263097.2:p.Thr252Met
ENST00000348419.7:c.638C>T	ENSP00000340129.2:p.Thr213Met
ENST00000562958.6:c.818C>T	ENSP00000456436.1:p.Thr273Met
ENST00000564572.1:n.927C>T
ENST00000565096.6:c.722C>T	ENSP00000457968.1:p.Thr241Met
ENST00000566695.5:c.566C>T	ENSP00000484533.1:p.Thr189Met
ENST00000568865.2:c.748C>T	ENSP00000458137.1:n.748C>T
NM_001303499.1:c.722C>T	NP_001290428.1:p.Thr241Met
NM_001303501.1:c.818C>T	NP_001290430.1:p.Thr273Met
NM_004368.3:c.755C>T	NP_004359.1:p.Thr252Met
NM_201277.2:c.638C>T	NP_958434.1:p.Thr213Met
NM_004368.4:c.755C>T MANE Select	NP_004359.1:p.Thr252Met
NM_001303499.2:c.722C>T	NP_001290428.1:p.Thr241Met
NM_001303501.2:c.818C>T	NP_001290430.1:p.Thr273Met
NM_201277.3:c.638C>T	NP_958434.1:p.Thr213Met