Canonical Allele Identifier: CA14743438
Gene: CPAMD8 HGNC NCBI

Linked Data

dbSNP Id: rs11666377
gnomAD v2: 19-17118433-C-T
gnomAD v3: 19-17007623-C-T
gnomAD v4: 19-17007623-C-T
MyVariant Identifiers: chr19:g.17118433C>T (hg19) chr19:g.17007623C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17007623C>T , CM000681.2:g.17007623C>T GRCh38
NC_000019.9:g.17118433C>T , CM000681.1:g.17118433C>T GRCh37
NC_000019.8:g.16979433C>T NCBI36
NG_054892.1:g.24196G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000651564.2:c.559+882G>A ENSP00000498697.2:n.559+882G>A
ENST00000291440.4:c.559+882G>A ENSP00000291440.4:n.559+882G>A
ENST00000443236.7:c.559+882G>A MANE Select ENSP00000402505.3:n.559+882G>A
ENST00000651564.1:c.700+882G>A ENSP00000498697.1:n.700+882G>A
ENST00000291440.3:c.700+882G>A ENSP00000291440.3:n.700+882G>A
ENST00000388925.8:c.559+882G>A ENSP00000373577.4:n.559+882G>A
ENST00000443236.5:c.700+882G>A ENSP00000402505.2:n.700+882G>A
NM_015692.2:c.700+882G>A NP_056507.2:n.700+882G>A
XM_011527917.1:c.664+882G>A XP_011526219.1:n.664+882G>A
XM_011527918.1:c.700+882G>A XP_011526220.1:n.700+882G>A
XM_011527919.1:c.700+882G>A XP_011526221.1:n.700+882G>A
XM_011527920.1:c.700+882G>A XP_011526222.1:n.700+882G>A
XM_011527921.1:c.700+882G>A XP_011526223.1:n.700+882G>A
XM_011527922.1:c.700+882G>A XP_011526224.1:n.700+882G>A
XM_011527923.1:c.700+882G>A XP_011526225.1:n.700+882G>A
XM_011527924.1:c.700+882G>A XP_011526226.1:n.700+882G>A
NM_015692.4:c.559+882G>A NP_056507.3:n.559+882G>A
XM_011527920.2:c.700+882G>A XP_011526222.1:n.700+882G>A
XM_011527921.3:c.700+882G>A XP_011526223.1:n.700+882G>A
XM_011527924.2:c.700+882G>A XP_011526226.1:n.700+882G>A
XM_017026594.1:c.700+882G>A XP_016882083.1:n.700+882G>A
NM_015692.5:c.559+882G>A MANE Select NP_056507.3:n.559+882G>A
NR_165644.1:n.727+882G>A
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