Canonical Allele Identifier: CA448963496

Gene: KAAG1 DCDC2

Linked Data

• MyVariant Identifiers: chr6:g.24357760T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24357532T>G , CM000668.2:g.24357532T>G	GRCh38
NC_000006.11:g.24357760T>G , CM000668.1:g.24357760T>G	GRCh37
NC_000006.10:g.24465739T>G	NCBI36
NG_012829.1:g.5521A>C
NG_012829.2:g.30761A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000274766.2:c.-108T>G (KAAG1)	ENSP00000274766.1:n.-108T>G
ENST00000378454.8:c.219A>C (DCDC2) MANE Select	ENSP00000367715.3:p.Arg73=
ENST00000274766.1:c.-108T>G (KAAG1)	ENSP00000274766.1:n.-108T>G
ENST00000378454.7:c.219A>C (DCDC2)	ENSP00000367715.3:p.Arg73=
ENST00000436313.1:c.122A>C (DCDC2)
NM_001195610.1:c.219A>C (DCDC2)	NP_001182539.1:p.Arg73=
NM_016356.4:c.219A>C (DCDC2)	NP_057440.2:p.Arg73=
NM_181337.3:c.-108T>G (KAAG1)	NP_851854.1:n.-108T>G
NM_016356.5:c.219A>C (DCDC2) MANE Select	NP_057440.2:p.Arg73=
NM_181337.4:c.-108T>G (KAAG1)	NP_851854.1:n.-108T>G
NM_001195610.2:c.219A>C (DCDC2)	NP_001182539.1:p.Arg73=
NR_174942.1:n.630T>G (KAAG1)