Canonical Allele Identifier: CA408649096

Gene: ASIP AHCY

Linked Data

• MyVariant Identifiers: chr20:g.32856967C>G (hg19) ; chr20:g.34269161C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34269161C>G , CM000682.2:g.34269161C>G	GRCh38
NC_000020.10:g.32856967C>G , CM000682.1:g.32856967C>G	GRCh37
NC_000020.9:g.32320628C>G	NCBI36
NG_011439.1:g.13797C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374954.4:c.393C>G (ASIP) MANE Select	ENSP00000364092.3:p.Asn131Lys
ENST00000374954.3:c.393C>G (ASIP)	ENSP00000364092.3:p.Asn131Lys
ENST00000568305.5:c.393C>G (ASIP)	ENSP00000454804.1:p.Asn131Lys
NM_001672.2:c.393C>G (ASIP)	NP_001663.2:p.Asn131Lys
XM_005260412.2:c.405C>G (ASIP)	XP_005260469.1:p.Asn135Lys
XM_011528657.1:c.*7+11866G>C (AHCY)	XP_011526959.1:n.*7+11866G>C
XM_011528820.1:c.393C>G (ASIP)	XP_011527122.1:p.Asn131Lys
XM_011528821.1:c.393C>G (ASIP)	XP_011527123.1:p.Asn131Lys
XM_011528822.1:c.393C>G (ASIP)	XP_011527124.1:p.Asn131Lys
XM_011528823.1:c.393C>G (ASIP)	XP_011527125.1:p.Asn131Lys
XM_005260412.3:c.405C>G (ASIP)	XP_005260469.1:p.Asn135Lys
XM_011528657.2:c.*7+11866G>C (AHCY)	XP_011526959.2:n.*7+11866G>C
XM_011528820.2:c.393C>G (ASIP)	XP_011527122.1:p.Asn131Lys
NM_001385218.1:c.393C>G (ASIP)	NP_001372147.1:p.Asn131Lys
NM_001672.3:c.393C>G (ASIP) MANE Select	NP_001663.2:p.Asn131Lys