Canonical Allele Identifier: CA1251629039

Gene: ACYP2

Linked Data

• dbSNP Id: rs1682111

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.54200842A>C , CM000664.2:g.54200842A>C	GRCh38
NC_000002.11:g.54427979A>C , CM000664.1:g.54427979A>C	GRCh37
NC_000002.10:g.54281483A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000394666.9:c.185+62094A>C MANE Select	ENSP00000378161.3:n.185+62094A>C
ENST00000394666.8:c.185+62094A>C	ENSP00000378161.3:n.185+62094A>C
ENST00000607452.6:c.404+62094A>C	ENSP00000475986.1:n.404+62094A>C
ENST00000303536.8:c.269+62094A>C	ENSP00000306448.4:n.269+62094A>C
ENST00000394666.7:c.185+62094A>C	ENSP00000378161.3:n.185+62094A>C
ENST00000494922.6:c.179-22155A>C
ENST00000606865.1:c.137+62094A>C	ENSP00000475333.1:n.137+62094A>C
ENST00000607452.5:c.404+62094A>C	ENSP00000475986.1:n.404+62094A>C
NM_138448.3:c.185+62094A>C	NP_612457.1:n.185+62094A>C
NM_001320586.1:c.404+62094A>C	NP_001307515.1:n.404+62094A>C
NM_001320587.1:c.311+62094A>C	NP_001307516.1:n.311+62094A>C
NM_001320588.1:c.113+62094A>C	NP_001307517.1:n.113+62094A>C
NM_001320589.1:c.185+62094A>C	NP_001307518.1:n.185+62094A>C
XM_017005411.1:c.485+62094A>C	XP_016860900.1:n.485+62094A>C
XM_017005412.1:c.485+62094A>C	XP_016860901.1:n.485+62094A>C
XM_017005413.1:c.*22+53410A>C	XP_016860902.1:n.*22+53410A>C
XR_001739083.1:n.1006-22155A>C
NM_001320586.2:c.404+62094A>C	NP_001307515.1:n.404+62094A>C
NM_001320587.2:c.311+62094A>C	NP_001307516.1:n.311+62094A>C
NM_001320588.2:c.113+62094A>C	NP_001307517.1:n.113+62094A>C
NM_001320589.2:c.185+62094A>C	NP_001307518.1:n.185+62094A>C
NM_138448.4:c.185+62094A>C MANE Select	NP_612457.1:n.185+62094A>C