Canonical Allele Identifier: CA510271189

Gene: ASIP AHCY

Linked Data

• MyVariant Identifiers: chr20:g.32856865C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34269059C>G , CM000682.2:g.34269059C>G	GRCh38
NC_000020.10:g.32856865C>G , CM000682.1:g.32856865C>G	GRCh37
NC_000020.9:g.32320526C>G	NCBI36
NG_011439.1:g.13695C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374954.4:c.291C>G (ASIP) MANE Select	ENSP00000364092.3:p.Arg97=
ENST00000374954.3:c.291C>G (ASIP)	ENSP00000364092.3:p.Arg97=
ENST00000568305.5:c.291C>G (ASIP)	ENSP00000454804.1:p.Arg97=
NM_001672.2:c.291C>G (ASIP)	NP_001663.2:p.Arg97=
XM_005260412.2:c.303C>G (ASIP)	XP_005260469.1:p.Arg101=
XM_011528657.1:c.*7+11968G>C (AHCY)	XP_011526959.1:n.*7+11968G>C
XM_011528820.1:c.291C>G (ASIP)	XP_011527122.1:p.Arg97=
XM_011528821.1:c.291C>G (ASIP)	XP_011527123.1:p.Arg97=
XM_011528822.1:c.291C>G (ASIP)	XP_011527124.1:p.Arg97=
XM_011528823.1:c.291C>G (ASIP)	XP_011527125.1:p.Arg97=
XM_005260412.3:c.303C>G (ASIP)	XP_005260469.1:p.Arg101=
XM_011528657.2:c.*7+11968G>C (AHCY)	XP_011526959.2:n.*7+11968G>C
XM_011528820.2:c.291C>G (ASIP)	XP_011527122.1:p.Arg97=
NM_001385218.1:c.291C>G (ASIP)	NP_001372147.1:p.Arg97=
NM_001672.3:c.291C>G (ASIP) MANE Select	NP_001663.2:p.Arg97=