Canonical Allele Identifier: CA2556808064

Gene: NR3C1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.143407174_143407175insAA , CM000667.2:g.143407174_143407175insAA	GRCh38
NC_000005.9:g.142786739_142786740insAA , CM000667.1:g.142786739_142786740insAA	GRCh37
NC_000005.8:g.142766932_142766933insAA	NCBI36
NG_009062.1:g.33338_33339insTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000343796.6:c.-13-6323_-13-6322insTT	ENSP00000343205.2:n.-13-6323_-13-6322insT...
ENST00000504572.5:c.-13-6323_-13-6322insTT	ENSP00000422518.1:n.-13-6323_-13-6322insT...
NM_001018074.1:c.-13-6323_-13-6322insTT	NP_001018084.1:n.-13-6323_-13-6322insTT
NM_001018075.1:c.-13-6323_-13-6322insTT	NP_001018085.1:n.-13-6323_-13-6322insTT
NM_001018077.1:c.-13-6323_-13-6322insTT	NP_001018087.1:n.-13-6323_-13-6322insTT
XM_005268422.2:c.-13-6323_-13-6322insTT	XP_005268479.1:n.-13-6323_-13-6322insTT
XM_005268422.3:c.-13-6323_-13-6322insTT	XP_005268479.1:n.-13-6323_-13-6322insTT
NM_001364183.1:c.-13-6323_-13-6322insTT	NP_001351112.1:n.-13-6323_-13-6322insTT
NM_001364183.2:c.-13-6323_-13-6322insTT	NP_001351112.1:n.-13-6323_-13-6322insTT