Canonical Allele Identifier: CA743840303

Gene: ASIP AHCY

Linked Data

• dbSNP Id: rs1465516696
• MyVariant Identifiers: chr20:g.32856646_32856647insCCC (hg19) ; chr20:g.34268840_34268841insCCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34268841_34268842insCCC , CM000682.2:g.34268841_34268842insCCC	GRCh38
NC_000020.10:g.32856647_32856648insCCC , CM000682.1:g.32856647_32856648insCCC	GRCh37
NC_000020.9:g.32320308_32320309insCCC	NCBI36
NG_011439.1:g.13477_13478insCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374954.4:c.223-150_223-149insCCC (ASIP) MANE Select	ENSP00000364092.3:n.223-150_223-149insCCC
ENST00000374954.3:c.223-150_223-149insCCC (ASIP)	ENSP00000364092.3:n.223-150_223-149insCCC
ENST00000568305.5:c.223-150_223-149insCCC (ASIP)	ENSP00000454804.1:n.223-150_223-149insCCC
NM_001672.2:c.223-150_223-149insCCC (ASIP)	NP_001663.2:n.223-150_223-149insCCC
XM_005260412.2:c.235-150_235-149insCCC (ASIP)	XP_005260469.1:n.235-150_235-149insCCC
XM_011528657.1:c.*7+12186_*7+12187insGGG (AHCY)	XP_011526959.1:n.*7+12186_*7+12187insGGG
XM_011528820.1:c.223-150_223-149insCCC (ASIP)	XP_011527122.1:n.223-150_223-149insCCC
XM_011528821.1:c.223-150_223-149insCCC (ASIP)	XP_011527123.1:n.223-150_223-149insCCC
XM_011528822.1:c.223-150_223-149insCCC (ASIP)	XP_011527124.1:n.223-150_223-149insCCC
XM_011528823.1:c.223-150_223-149insCCC (ASIP)	XP_011527125.1:n.223-150_223-149insCCC
XM_005260412.3:c.235-150_235-149insCCC (ASIP)	XP_005260469.1:n.235-150_235-149insCCC
XM_011528657.2:c.*7+12186_*7+12187insGGG (AHCY)	XP_011526959.2:n.*7+12186_*7+12187insGGG
XM_011528820.2:c.223-150_223-149insCCC (ASIP)	XP_011527122.1:n.223-150_223-149insCCC
NM_001385218.1:c.223-150_223-149insCCC (ASIP)	NP_001372147.1:n.223-150_223-149insCCC
NM_001672.3:c.223-150_223-149insCCC (ASIP) MANE Select	NP_001663.2:n.223-150_223-149insCCC