Canonical Allele Identifier: CA3017190

Gene: RAP1GDS1

Linked Data

• dbSNP Id: rs776791878
• ExAC: 4:99337890 C / G
• gnomAD v2: 4-99337890-C-G
• gnomAD v4: 4-98416739-C-G
• MyVariant Identifiers: chr4:g.99337890C>G (hg19) ; chr4:g.98416739C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.98416739C>G , CM000666.2:g.98416739C>G	GRCh38
NC_000004.11:g.99337890C>G , CM000666.1:g.99337890C>G	GRCh37
NC_000004.10:g.99556913C>G	NCBI36

Transcript Alleles

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