Canonical Allele Identifier: CA1365277741

Gene: DCP1A CACNA1D

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53344218C>G , CM000665.2:g.53344218C>G	GRCh38
NC_000003.11:g.53378245C>G , CM000665.1:g.53378245C>G	GRCh37
NC_000003.10:g.53353285C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_018403.7:c.176+684G>C (DCP1A) MANE Select	NP_060873.4:n.176+684G>C
ENST00000610213.6:c.176+684G>C (DCP1A) MANE Select	ENSP00000476386.1:n.176+684G>C
NM_001290204.1:c.176+684G>C (DCP1A)	NP_001277133.1:n.176+684G>C
NM_001290204.2:c.176+684G>C (DCP1A)	NP_001277133.1:n.176+684G>C
NM_001290205.1:c.-96+684G>C (DCP1A)	NP_001277134.1:n.-96+684G>C
NM_001290205.2:c.-96+684G>C (DCP1A)	NP_001277134.1:n.-96+684G>C
NM_001290206.1:c.-60+684G>C (DCP1A)	NP_001277135.1:n.-60+684G>C
NM_001290206.2:c.-60+684G>C (DCP1A)	NP_001277135.1:n.-60+684G>C
NM_001290207.1:c.-60+684G>C (DCP1A)	NP_001277136.1:n.-60+684G>C
NM_001290207.2:c.-60+684G>C (DCP1A)	NP_001277136.1:n.-60+684G>C
NM_018403.6:c.176+684G>C (DCP1A)	NP_060873.4:n.176+684G>C
ENST00000294241.10:c.176+684G>C (DCP1A)	ENSP00000476046.2:n.176+684G>C
ENST00000559748.5:c.170+684G>C (DCP1A)	ENSP00000479387.1:n.170+684G>C
ENST00000560076.2:c.176+684G>C (DCP1A)	ENSP00000480912.1:n.176+684G>C
ENST00000560624.5:c.137+684G>C (DCP1A)	ENSP00000477594.1:n.137+684G>C
ENST00000610213.5:c.176+684G>C (DCP1A)	ENSP00000476386.1:n.176+684G>C
ENST00000637424.1:c.139+14774C>G (CACNA1D)	ENSP00000489769.1:n.139+14774C>G