Canonical Allele Identifier: CA363278921

Gene: KAAG1 DCDC2

Linked Data

• MyVariant Identifiers: chr6:g.24357759T>G (hg19) ; chr6:g.24357531T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24357531T>G , CM000668.2:g.24357531T>G	GRCh38
NC_000006.11:g.24357759T>G , CM000668.1:g.24357759T>G	GRCh37
NC_000006.10:g.24465738T>G	NCBI36
NG_012829.1:g.5522A>C
NG_012829.2:g.30762A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000274766.2:c.-109T>G (KAAG1)	ENSP00000274766.1:n.-109T>G
ENST00000378454.8:c.220A>C (DCDC2) MANE Select	ENSP00000367715.3:p.Ile74Leu
ENST00000274766.1:c.-109T>G (KAAG1)	ENSP00000274766.1:n.-109T>G
ENST00000378454.7:c.220A>C (DCDC2)	ENSP00000367715.3:p.Ile74Leu
ENST00000436313.1:c.123A>C (DCDC2)
NM_001195610.1:c.220A>C (DCDC2)	NP_001182539.1:p.Ile74Leu
NM_016356.4:c.220A>C (DCDC2)	NP_057440.2:p.Ile74Leu
NM_181337.3:c.-109T>G (KAAG1)	NP_851854.1:n.-109T>G
NM_016356.5:c.220A>C (DCDC2) MANE Select	NP_057440.2:p.Ile74Leu
NM_181337.4:c.-109T>G (KAAG1)	NP_851854.1:n.-109T>G
NM_001195610.2:c.220A>C (DCDC2)	NP_001182539.1:p.Ile74Leu
NR_174942.1:n.629T>G (KAAG1)