Canonical Allele Identifier: CA2406161371

Gene: RANGAP1

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.41265150G>A , CM000684.2:g.41265150G>A	GRCh38
NC_000022.10:g.41661154G>A , CM000684.1:g.41661154G>A	GRCh37
NC_000022.9:g.39991100G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000705116.1:c.301-307C>T	ENSP00000516069.1:n.301-307C>T
ENST00000356244.8:c.301-307C>T MANE Select	ENSP00000348577.3:n.301-307C>T
ENST00000356244.7:c.301-307C>T	ENSP00000348577.3:n.301-307C>T
ENST00000405486.5:c.301-307C>T	ENSP00000385866.1:n.301-307C>T
ENST00000446258.5:c.122-307C>T
ENST00000452543.5:c.301-307C>T	ENSP00000394787.1:n.301-307C>T
ENST00000455915.6:c.301-307C>T	ENSP00000401470.2:n.301-307C>T
NM_001278651.1:c.301-307C>T	NP_001265580.1:n.301-307C>T
NM_002883.3:c.301-307C>T	NP_002874.1:n.301-307C>T
XM_005261695.1:c.466-307C>T	XP_005261752.1:n.466-307C>T
XM_005261696.1:c.424-307C>T	XP_005261753.1:n.424-307C>T
XM_006724289.2:c.301-307C>T	XP_006724352.1:n.301-307C>T
XM_011530293.1:c.466-307C>T	XP_011528595.1:n.466-307C>T
XM_011530294.1:c.301-307C>T	XP_011528596.1:n.301-307C>T
XM_011530295.1:c.301-307C>T	XP_011528597.1:n.301-307C>T
XM_011530296.1:c.301-307C>T	XP_011528598.1:n.301-307C>T
XM_011530297.1:c.466-307C>T	XP_011528599.1:n.466-307C>T
NM_001317930.1:c.301-307C>T	NP_001304859.1:n.301-307C>T
XM_006724289.4:c.301-307C>T	XP_006724352.1:n.301-307C>T
XM_011530294.3:c.301-307C>T	XP_011528596.1:n.301-307C>T
XM_011530295.2:c.301-307C>T	XP_011528597.1:n.301-307C>T
XM_017028893.2:c.301-307C>T	XP_016884382.1:n.301-307C>T
XM_017028894.2:c.301-307C>T	XP_016884383.1:n.301-307C>T
XM_017028895.2:c.301-307C>T	XP_016884384.1:n.301-307C>T
XM_017028896.2:c.301-307C>T	XP_016884385.1:n.301-307C>T
XM_017028897.1:c.301-307C>T	XP_016884386.1:n.301-307C>T
XM_017028898.2:c.202-307C>T	XP_016884387.1:n.202-307C>T
XM_017028899.1:c.301-307C>T	XP_016884388.1:n.301-307C>T
XR_002958711.1:n.757-307C>T
NM_001278651.2:c.301-307C>T	NP_001265580.1:n.301-307C>T
NM_001317930.2:c.301-307C>T	NP_001304859.1:n.301-307C>T
NM_002883.4:c.301-307C>T MANE Select	NP_002874.1:n.301-307C>T