Canonical Allele Identifier: CA1192293736

Gene: HSD3B2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119422897_119422901delinsTTAAC , CM000663.2:g.119422897_119422901delinsTTAAC	GRCh38
NC_000001.10:g.119965520_119965524delinsTTAAC , CM000663.1:g.119965520_119965524delinsTTAAC	GRCh37
NC_000001.9:g.119767043_119767047delinsTTAAC	NCBI36
NG_013349.1:g.12967_12971delinsTTAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369416.4:c.*277_*281delinsTTAAC MANE Select	ENSP00000358424.3:n.*277_*281delinsTTAAC
ENST00000369416.3:c.*277_*281delinsTTAAC	ENSP00000358424.3:n.*277_*281delinsTTAAC
ENST00000543831.5:c.*277_*281delinsTTAAC	ENSP00000445122.1:n.*277_*281delinsTTAAC
NM_000198.3:c.*277_*281delinsTTAAC	NP_000189.1:n.*277_*281delinsTTAAC
NM_001166120.1:c.*277_*281delinsTTAAC	NP_001159592.1:n.*277_*281delinsTTAAC
NM_000198.4:c.*277_*281delinsTTAAC MANE Select	NP_000189.1:n.*277_*281delinsTTAAC
NM_001166120.2:c.*277_*281delinsTTAAC	NP_001159592.1:n.*277_*281delinsTTAAC