Canonical Allele Identifier: CA2671483037

Gene: RAP1GDS1

Linked Data

• gnomAD v4: 4-98416634-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.98416634G>T , CM000666.2:g.98416634G>T	GRCh38
NC_000004.11:g.99337785G>T , CM000666.1:g.99337785G>T	GRCh37
NC_000004.10:g.99556808G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000408927.8:c.764-111G>T MANE Select	ENSP00000386153.4:n.764-111G>T
ENST00000264572.11:c.491-111G>T	ENSP00000264572.7:n.491-111G>T
ENST00000339360.9:c.767-111G>T	ENSP00000340454.5:n.767-111G>T
ENST00000380158.8:c.620-111G>T	ENSP00000369503.4:n.620-111G>T
ENST00000408900.7:c.617-111G>T	ENSP00000386223.3:n.617-111G>T
ENST00000408927.7:c.764-111G>T	ENSP00000386153.3:n.764-111G>T
ENST00000453712.6:c.767-111G>T	ENSP00000407157.2:n.767-111G>T
ENST00000509501.5:c.192-111G>T
NM_001100426.1:c.767-111G>T	NP_001093896.1:n.767-111G>T
NM_001100427.1:c.764-111G>T	NP_001093897.1:n.764-111G>T
NM_001100428.1:c.620-111G>T	NP_001093898.1:n.620-111G>T
NM_001100429.1:c.617-111G>T	NP_001093899.1:n.617-111G>T
NM_001100430.1:c.491-111G>T	NP_001093900.1:n.491-111G>T
NM_021159.4:c.767-111G>T	NP_066982.3:n.767-111G>T
XM_006714284.2:c.524-111G>T	XP_006714347.1:n.524-111G>T
XM_006714285.2:c.377-111G>T	XP_006714348.1:n.377-111G>T
XM_011532173.1:c.767-111G>T	XP_011530475.1:n.767-111G>T
XM_024454164.1:c.764-111G>T	XP_024309932.1:n.764-111G>T
XM_024454165.1:c.620-111G>T	XP_024309933.1:n.620-111G>T
XM_024454166.1:c.617-111G>T	XP_024309934.1:n.617-111G>T
XM_024454167.1:c.524-111G>T	XP_024309935.1:n.524-111G>T
XM_024454168.1:c.524-111G>T	XP_024309936.1:n.524-111G>T
XM_024454169.1:c.377-111G>T	XP_024309937.1:n.377-111G>T
XM_024454170.1:c.377-111G>T	XP_024309938.1:n.377-111G>T
XM_024454171.1:c.377-111G>T	XP_024309939.1:n.377-111G>T
XM_024454172.1:c.377-111G>T	XP_024309940.1:n.377-111G>T
XM_024454173.1:c.377-111G>T	XP_024309941.1:n.377-111G>T
XM_024454174.1:c.230-111G>T	XP_024309942.1:n.230-111G>T
XM_024454175.1:c.230-111G>T	XP_024309943.1:n.230-111G>T
XM_024454176.1:c.230-111G>T	XP_024309944.1:n.230-111G>T
XR_002959742.1:n.945-111G>T
XR_002959743.1:n.805-111G>T
XR_002959744.1:n.802-111G>T
NM_001100426.2:c.767-111G>T	NP_001093896.1:n.767-111G>T
NM_001100427.2:c.764-111G>T MANE Select	NP_001093897.1:n.764-111G>T
NM_001100428.2:c.620-111G>T	NP_001093898.1:n.620-111G>T
NM_001100429.2:c.617-111G>T	NP_001093899.1:n.617-111G>T
NM_001100430.2:c.491-111G>T	NP_001093900.1:n.491-111G>T
NM_021159.5:c.767-111G>T	NP_066982.3:n.767-111G>T