Canonical Allele Identifier: CA1611100453

Gene: PHACTR1

Linked Data

• dbSNP Id: rs1788366013

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.12927224T>A , CM000668.2:g.12927224T>A	GRCh38
NC_000006.11:g.12927456T>A , CM000668.1:g.12927456T>A	GRCh37
NC_000006.10:g.13035442T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000689548.1:c.113-126141T>A	ENSP00000509837.1:n.113-126141T>A
ENST00000692662.1:n.409-126141T>A
ENST00000693693.1:n.1117-126141T>A
ENST00000332995.12:c.251-126141T>A MANE Select	ENSP00000329880.8:n.251-126141T>A
ENST00000379348.3:n.428-6409T>A
ENST00000406205.7:c.113-126141T>A	ENSP00000384760.3:n.113-126141T>A
ENST00000674595.1:c.251-126141T>A	ENSP00000502157.1:n.251-126141T>A
ENST00000674637.1:c.251-126141T>A	ENSP00000501634.1:n.251-126141T>A
ENST00000676159.1:c.251-126141T>A	ENSP00000501921.1:n.251-126141T>A
ENST00000332995.11:c.251-126141T>A	ENSP00000329880.8:n.251-126141T>A
ENST00000379348.2:c.251-6409T>A	ENSP00000368653.2:n.251-6409T>A
ENST00000379350.5:c.251-126141T>A	ENSP00000368655.1:n.251-126141T>A
ENST00000406205.6:c.357-126141T>A
NM_001242648.1:c.251-126141T>A	NP_001229577.1:n.251-126141T>A
NM_030948.2:c.251-126141T>A	NP_112210.1:n.251-126141T>A
XM_005248933.1:c.251-126141T>A	XP_005248990.1:n.251-126141T>A
XM_005248934.1:c.251-126141T>A	XP_005248991.1:n.251-126141T>A
XM_005248935.3:c.251-126141T>A	XP_005248992.1:n.251-126141T>A
XM_011514390.1:c.251-126141T>A	XP_011512692.1:n.251-126141T>A
NM_001242648.2:c.251-126141T>A	NP_001229577.1:n.251-126141T>A
NM_001322308.1:c.251-126141T>A	NP_001309237.1:n.251-126141T>A
NM_001322309.1:c.251-126141T>A	NP_001309238.1:n.251-126141T>A
NM_001322310.1:c.251-126141T>A	NP_001309239.1:n.251-126141T>A
NM_030948.3:c.251-126141T>A	NP_112210.1:n.251-126141T>A
XM_005248934.3:c.251-126141T>A	XP_005248991.1:n.251-126141T>A
XM_017010454.2:c.251-126141T>A	XP_016865943.1:n.251-126141T>A
XM_017010455.2:c.251-126141T>A	XP_016865944.1:n.251-126141T>A
XM_017010456.2:c.251-126141T>A	XP_016865945.1:n.251-126141T>A
XM_017010457.2:c.251-126141T>A	XP_016865946.1:n.251-126141T>A
XM_017010459.2:c.251-126141T>A	XP_016865948.1:n.251-126141T>A
XM_017010460.2:c.251-126141T>A	XP_016865949.1:n.251-126141T>A
XM_017010461.2:c.251-126141T>A	XP_016865950.1:n.251-126141T>A
XM_017010462.2:c.251-126141T>A	XP_016865951.1:n.251-126141T>A
NM_001242648.3:c.251-126141T>A	NP_001229577.1:n.251-126141T>A
NM_001322308.2:c.251-126141T>A	NP_001309237.1:n.251-126141T>A
NM_001322309.2:c.251-126141T>A	NP_001309238.1:n.251-126141T>A
NM_001374581.1:c.251-126141T>A	NP_001361510.1:n.251-126141T>A
NM_001374582.1:c.251-126141T>A	NP_001361511.1:n.251-126141T>A
NM_030948.5:c.251-126141T>A	NP_112210.1:n.251-126141T>A
NM_001242648.4:c.251-126141T>A	NP_001229577.1:n.251-126141T>A
NM_001322308.3:c.251-126141T>A	NP_001309237.1:n.251-126141T>A
NM_001322309.3:c.251-126141T>A	NP_001309238.1:n.251-126141T>A
NM_001322310.2:c.251-126141T>A	NP_001309239.1:n.251-126141T>A
NM_001374581.2:c.251-126141T>A	NP_001361510.1:n.251-126141T>A
NM_030948.6:c.251-126141T>A MANE Select	NP_112210.1:n.251-126141T>A