Canonical Allele Identifier: CA354709486

Gene: RAB7A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128807625A>T , CM000665.2:g.128807625A>T	GRCh38
NC_000003.11:g.128526468A>T , CM000665.1:g.128526468A>T	GRCh37
NC_000003.10:g.130009158A>T	NCBI36
NG_008070.1:g.86490A>T , LRG_266:g.86490A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004637.6:c.482A>T MANE Select	NP_004628.4:p.Asn161Ile
ENST00000265062.8:c.482A>T MANE Select	ENSP00000265062.3:p.Asn161Ile
NM_004637.5:c.482A>T , LRG_266t1:c.482A>T	NP_004628.4:p.Asn161Ile
ENST00000265062.7:c.482A>T	ENSP00000265062.3:p.Asn161Ile
ENST00000482525.5:c.341A>T	ENSP00000417668.1:p.Asn114Ile
ENST00000483906.5:c.263A>T	ENSP00000417155.1:p.Asn88Ile
ENST00000485280.1:c.181-5702A>T	ENSP00000418283.1:n.181-5702A>T
ENST00000490093.6:c.*24A>T	ENSP00000418955.2:n.*24A>T
ENST00000493186.5:c.155A>T	ENSP00000417189.1:p.Asn52Ile
ENST00000493186.6:c.155A>T	ENSP00000417189.1:p.Asn52Ile
ENST00000674589.1:c.482A>T	ENSP00000502088.1:p.Asn161Ile
ENST00000674593.1:n.480A>T
ENST00000674748.1:c.410A>T	ENSP00000502224.1:p.Asn137Ile
ENST00000675342.1:c.482A>T	ENSP00000502486.1:p.Asn161Ile
ENST00000675497.1:c.482A>T	ENSP00000502000.1:p.Asn161Ile
ENST00000675712.1:n.1666A>T
ENST00000675864.1:c.482A>T	ENSP00000502566.1:p.Asn161Ile
ENST00000676147.1:c.562A>T
ENST00000676214.1:c.482A>T	ENSP00000501618.1:p.Asn161Ile
ENST00000676425.1:c.482A>T	ENSP00000502084.1:p.Asn161Ile
XM_024453745.1:c.482A>T	XP_024309513.1:p.Asn161Ile
XR_002959582.1:n.1666A>T
XR_002959583.1:n.1594A>T