Canonical Allele Identifier: CA2658939754
Gene: CALM2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47162421_47162452dup , CM000664.2:g.47162421_47162452dup GRCh38
NC_000002.11:g.47389560_47389591dup , CM000664.1:g.47389560_47389591dup GRCh37
NC_000002.10:g.47243064_47243095dup NCBI36
NG_042065.1:g.19490_19521dup

Transcript Alleles

HGVS Amino-acid change
ENST00000272298.12:c.179-55_179-24dup MANE Select ENSP00000272298.7:n.179-55_179-24dup
ENST00000456319.6:c.71-55_71-24dup ENSP00000411440.2:n.71-55_71-24dup
ENST00000652974.1:c.*163-55_*163-24dup ENSP00000499369.1:n.*163-55_*163-24dup
ENST00000655450.1:c.71-55_71-24dup ENSP00000499266.1:n.71-55_71-24dup
ENST00000655728.1:c.71-55_71-24dup ENSP00000499656.1:n.71-55_71-24dup
ENST00000656538.1:c.71-55_71-24dup ENSP00000499357.1:n.71-55_71-24dup
ENST00000668667.1:c.71-55_71-24dup ENSP00000499706.1:n.71-55_71-24dup
ENST00000670593.1:n.1084-55_1084-24dup
ENST00000272298.11:c.179-55_179-24dup ENSP00000272298.7:n.179-55_179-24dup
ENST00000409563.5:c.320-55_320-24dup ENSP00000387065.1:n.320-55_320-24dup
ENST00000422269.1:c.102+8287_102+8318dup
ENST00000432899.5:c.178+72_178+103dup ENSP00000406112.1:n.178+72_178+103dup
ENST00000456319.5:c.293-55_293-24dup ENSP00000411440.1:n.293-55_293-24dup
ENST00000460218.5:n.3619-55_3619-24dup
ENST00000482532.5:n.1446-55_1446-24dup
ENST00000484408.5:n.440-55_440-24dup
ENST00000489742.1:n.416-55_416-24dup
ENST00000628793.2:c.165+85_165+116dup ENSP00000486952.1:n.165+85_165+116dup
NM_001305624.1:c.323-55_323-24dup NP_001292553.1:n.323-55_323-24dup
NM_001305625.1:c.71-55_71-24dup NP_001292554.1:n.71-55_71-24dup
NM_001305626.1:c.71-55_71-24dup NP_001292555.1:n.71-55_71-24dup
NM_001743.4:c.179-55_179-24dup NP_001734.1:n.179-55_179-24dup
NM_001743.5:c.179-55_179-24dup NP_001734.1:n.179-55_179-24dup
NM_001743.6:c.179-55_179-24dup MANE Select NP_001734.1:n.179-55_179-24dup
NM_001305625.2:c.71-55_71-24dup NP_001292554.1:n.71-55_71-24dup