Canonical Allele Identifier: CA2838236789

Gene: FAAP20

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2204590C>G , CM000663.2:g.2204590C>G	GRCh38
NC_000001.10:g.2136029C>G , CM000663.1:g.2136029C>G	GRCh37
NC_000001.9:g.2125889C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000469733.5:n.452-960G>C
ENST00000487186.5:n.260-960G>C
NM_001146310.1:c.-322-960G>C	NP_001139782.1:n.-322-960G>C
NM_001282670.1:c.-2304-960G>C	NP_001269599.1:n.-2304-960G>C
XM_011540914.1:c.126-960G>C	XP_011539216.1:n.126-960G>C
XM_011540915.1:c.126-960G>C	XP_011539217.1:n.126-960G>C
XM_011540916.1:c.126-960G>C	XP_011539218.1:n.126-960G>C
XM_011540917.1:c.126-960G>C	XP_011539219.1:n.126-960G>C
XM_011540918.1:c.126-960G>C	XP_011539220.1:n.126-960G>C
XM_011540919.1:c.126-960G>C	XP_011539221.1:n.126-960G>C
XM_011540920.1:c.126-960G>C	XP_011539222.1:n.126-960G>C
XM_011540914.2:c.126-960G>C	XP_011539216.1:n.126-960G>C
XM_017000553.1:c.90-960G>C	XP_016856042.1:n.90-960G>C
NM_001146310.2:c.-322-960G>C	NP_001139782.1:n.-322-960G>C
NM_001282670.2:c.-2304-960G>C	NP_001269599.1:n.-2304-960G>C