Canonical Allele Identifier: CA1278292701

Gene: RANBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108768421_108768425delinsTTTTC , CM000664.2:g.108768421_108768425delinsTTTTC	GRCh38
NC_000002.11:g.109384877_109384881delinsTTTTC , CM000664.1:g.109384877_109384881delinsTTTTC	GRCh37
NC_000002.10:g.108751309_108751313delinsTTTTC	NCBI36
NG_012210.1:g.53941_53945delinsTTTTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000697737.1:c.2603-3280_2603-3276delinsTTTTC	ENSP00000513426.1:n.2603-3280_2603-3276de...
ENST00000697740.1:c.2525-3280_2525-3276delinsTTTTC	ENSP00000513427.1:n.2525-3280_2525-3276de...
ENST00000697744.1:c.2715+33_2715+37delinsTTTTC
ENST00000697745.1:c.2715+33_2715+37delinsTTTTC
ENST00000697746.1:n.694_698delinsTTTTC
ENST00000697747.1:c.480+33_480+37delinsTTTTC
ENST00000697748.1:n.184_188delinsTTTTC
ENST00000283195.11:c.7849+33_7849+37delinsTTTTC MANE Select	ENSP00000283195.6:n.7849+33_7849+37delins...
ENST00000283195.10:c.7849+33_7849+37delinsTTTTC	ENSP00000283195.6:n.7849+33_7849+37delins...
NM_006267.4:c.7849+33_7849+37delinsTTTTC	NP_006258.3:n.7849+33_7849+37delinsTTTTC
XM_005264002.1:c.7849+33_7849+37delinsTTTTC	XP_005264059.1:n.7849+33_7849+37delinsTTT...
XM_005264003.1:c.7849+33_7849+37delinsTTTTC	XP_005264060.1:n.7849+33_7849+37delinsTTT...
XM_005264004.1:c.7849+33_7849+37delinsTTTTC	XP_005264061.1:n.7849+33_7849+37delinsTTT...
XM_005264005.3:c.7771+33_7771+37delinsTTTTC	XP_005264062.1:n.7771+33_7771+37delinsTTT...
XM_005264007.1:c.4921+33_4921+37delinsTTTTC	XP_005264064.1:n.4921+33_4921+37delinsTTT...
XM_011511575.1:c.7846+33_7846+37delinsTTTTC	XP_011509877.1:n.7846+33_7846+37delinsTTT...
XM_011511576.1:c.7672+33_7672+37delinsTTTTC	XP_011509878.1:n.7672+33_7672+37delinsTTT...
XM_011511577.1:c.5137+33_5137+37delinsTTTTC	XP_011509879.1:n.5137+33_5137+37delinsTTT...
XM_011511578.1:c.4918+33_4918+37delinsTTTTC	XP_011509880.1:n.4918+33_4918+37delinsTTT...
XM_005264002.3:c.7849+33_7849+37delinsTTTTC	XP_005264059.1:n.7849+33_7849+37delinsTTT...
XM_005264003.3:c.7849+33_7849+37delinsTTTTC	XP_005264060.1:n.7849+33_7849+37delinsTTT...
XM_005264004.3:c.7849+33_7849+37delinsTTTTC	XP_005264061.1:n.7849+33_7849+37delinsTTT...
XM_005264005.4:c.7771+33_7771+37delinsTTTTC	XP_005264062.1:n.7771+33_7771+37delinsTTT...
XM_005264007.3:c.4921+33_4921+37delinsTTTTC	XP_005264064.1:n.4921+33_4921+37delinsTTT...
XM_011511575.2:c.7846+33_7846+37delinsTTTTC	XP_011509877.1:n.7846+33_7846+37delinsTTT...
XM_011511576.3:c.7672+33_7672+37delinsTTTTC	XP_011509878.1:n.7672+33_7672+37delinsTTT...
XM_011511578.2:c.4918+33_4918+37delinsTTTTC	XP_011509880.1:n.4918+33_4918+37delinsTTT...
XM_017004623.2:c.7849+33_7849+37delinsTTTTC	XP_016860112.1:n.7849+33_7849+37delinsTTT...
NM_006267.5:c.7849+33_7849+37delinsTTTTC MANE Select	NP_006258.3:n.7849+33_7849+37delinsTTTTC