Canonical Allele Identifier: CA769425581

Gene: CALM2

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47171925C>A , CM000664.2:g.47171925C>A	GRCh38
NC_000002.11:g.47399064C>A , CM000664.1:g.47399064C>A	GRCh37
NC_000002.10:g.47252568C>A	NCBI36
NG_042065.1:g.10012G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272298.12:c.4-1161G>T MANE Select	ENSP00000272298.7:n.4-1161G>T
ENST00000456319.6:c.-106+489G>T	ENSP00000411440.2:n.-106+489G>T
ENST00000652974.1:c.102-1161G>T	ENSP00000499369.1:n.102-1161G>T
ENST00000655450.1:c.-105-1161G>T	ENSP00000499266.1:n.-105-1161G>T
ENST00000655728.1:c.-105-1161G>T	ENSP00000499656.1:n.-105-1161G>T
ENST00000656538.1:c.-105-1161G>T	ENSP00000499357.1:n.-105-1161G>T
ENST00000668667.1:c.-105-1161G>T	ENSP00000499706.1:n.-105-1161G>T
ENST00000272298.11:c.4-1161G>T	ENSP00000272298.7:n.4-1161G>T
ENST00000409563.5:c.-71-1161G>T	ENSP00000387065.1:n.-71-1161G>T
ENST00000422269.1:c.72-1161G>T
ENST00000432899.5:c.4-1161G>T	ENSP00000406112.1:n.4-1161G>T
ENST00000456319.5:c.117+489G>T	ENSP00000411440.1:n.117+489G>T
ENST00000460218.5:n.2283G>T
ENST00000484408.5:n.264+489G>T
ENST00000489742.1:n.240+489G>T
ENST00000628793.2:c.4-1161G>T	ENSP00000486952.1:n.4-1161G>T
NM_001305624.1:c.147+489G>T	NP_001292553.1:n.147+489G>T
NM_001305625.1:c.-105-1161G>T	NP_001292554.1:n.-105-1161G>T
NM_001305626.1:c.-1266G>T	NP_001292555.1:n.-1266G>T
NM_001743.4:c.4-1161G>T	NP_001734.1:n.4-1161G>T
NM_001743.5:c.4-1161G>T	NP_001734.1:n.4-1161G>T
NM_001743.6:c.4-1161G>T MANE Select	NP_001734.1:n.4-1161G>T
NM_001305625.2:c.-105-1161G>T	NP_001292554.1:n.-105-1161G>T