Canonical Allele Identifier: CA389871879

Gene: DAAM1

Linked Data

• MyVariant Identifiers: chr14:g.59819339T>A (hg19) ; chr14:g.59352621T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.59352621T>A , CM000676.2:g.59352621T>A	GRCh38
NC_000014.8:g.59819339T>A , CM000676.1:g.59819339T>A	GRCh37
NC_000014.7:g.58889092T>A	NCBI36
NG_047127.1:g.169011T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360909.8:c.2256T>A MANE Select	ENSP00000354162.3:p.Phe752Leu
ENST00000360909.7:c.2256T>A	ENSP00000354162.3:p.Phe752Leu
ENST00000395125.1:c.2286T>A	ENSP00000378557.1:p.Phe762Leu
ENST00000553966.5:n.173T>A
ENST00000554459.5:n.475T>A
NM_001270520.1:c.2256T>A	NP_001257449.1:p.Phe752Leu
NM_014992.2:c.2286T>A	NP_055807.1:p.Phe762Leu
XM_005267430.1:c.2286T>A	XP_005267487.1:p.Phe762Leu
XM_005267431.1:c.2286T>A	XP_005267488.1:p.Phe762Leu
XM_005267430.2:c.2286T>A	XP_005267487.1:p.Phe762Leu
NM_001270520.2:c.2256T>A MANE Select	NP_001257449.1:p.Phe752Leu