Canonical Allele Identifier: CA2691372602

Gene: WHRN

Linked Data

• gnomAD v4: 9-114406425-G-GTAGACGGCAGCTTGTCC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114406425_114406426insTAGACGGCAGCTTGTCC , CM000671.2:g.114406425_114406426insTAGACGGCAGCTTGTCC	GRCh38
NC_000009.11:g.117168705_117168706insTAGACGGCAGCTTGTCC , CM000671.1:g.117168705_117168706insTAGACGGCAGCTTGTCC	GRCh37
NC_000009.10:g.116208526_116208527insTAGACGGCAGCTTGTCC	NCBI36
NG_016700.1:g.104031_104032insGGACAAGCTGCCGTCTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000699485.1:c.509_510insGGACAAGCTGCCGTCTA	ENSP00000514396.1:p.Met171AspfsTer22
ENST00000362057.4:c.2165_2166insGGACAAGCTGCCGTCTA MANE Select	ENSP00000354623.3:p.Met723AspfsTer22
ENST00000674036.8:c.1138_1139insGGACAAGCTGCCGTCTA
ENST00000674048.1:n.2046_2047insGGACAAGCTGCCGTCTA
ENST00000265134.10:c.1016_1017insGGACAAGCTGCCGTCTA	ENSP00000265134.6:p.Met340AspfsTer22
ENST00000362057.3:c.2165_2166insGGACAAGCTGCCGTCTA	ENSP00000354623.3:p.Met723AspfsTer22
ENST00000374059.7:c.1112_1113insGGACAAGCTGCCGTCTA	ENSP00000363172.3:p.Met372AspfsTer22
NM_001083885.2:c.1016_1017insGGACAAGCTGCCGTCTA	NP_001077354.2:p.Met340AspfsTer22
NM_001173425.1:c.2165_2166insGGACAAGCTGCCGTCTA	NP_001166896.1:p.Met723AspfsTer22
NM_015404.3:c.2165_2166insGGACAAGCTGCCGTCTA	NP_056219.3:p.Met723AspfsTer22
XM_005251897.3:c.1502_1503insGGACAAGCTGCCGTCTA	XP_005251954.2:p.Met502AspfsTer22
XM_011518484.1:c.2198_2199insGGACAAGCTGCCGTCTA	XP_011516786.1:p.Met734AspfsTer22
XM_011518485.1:c.2198_2199insGGACAAGCTGCCGTCTA	XP_011516787.1:p.Met734AspfsTer22
XM_011518486.1:c.2198_2199insGGACAAGCTGCCGTCTA	XP_011516788.1:p.Met734AspfsTer22
XM_011518487.1:c.2072_2073insGGACAAGCTGCCGTCTA	XP_011516789.1:p.Met692AspfsTer22
XM_011518488.1:c.1955_1956insGGACAAGCTGCCGTCTA	XP_011516790.1:p.Met653AspfsTer22
XM_011518495.1:c.875_876insGGACAAGCTGCCGTCTA	XP_011516797.1:p.Met293AspfsTer22
XR_929747.1:n.3102_3103insGGACAAGCTGCCGTCTA
XR_929748.1:n.3000_3001insGGACAAGCTGCCGTCTA
NM_001346890.1:c.1112_1113insGGACAAGCTGCCGTCTA	NP_001333819.1:p.Met372AspfsTer22
XM_011518486.2:c.2198_2199insGGACAAGCTGCCGTCTA	XP_011516788.1:p.Met734AspfsTer22
XM_011518487.2:c.2072_2073insGGACAAGCTGCCGTCTA	XP_011516789.1:p.Met692AspfsTer22
XM_011518488.2:c.1955_1956insGGACAAGCTGCCGTCTA	XP_011516790.1:p.Met653AspfsTer22
XR_929747.2:n.2413_2414insGGACAAGCTGCCGTCTA
XR_929748.2:n.2311_2312insGGACAAGCTGCCGTCTA
NM_015404.4:c.2165_2166insGGACAAGCTGCCGTCTA MANE Select	NP_056219.3:p.Met723AspfsTer22
NM_001173425.2:c.2165_2166insGGACAAGCTGCCGTCTA	NP_001166896.1:p.Met723AspfsTer22
NM_001083885.3:c.1016_1017insGGACAAGCTGCCGTCTA	NP_001077354.2:p.Met340AspfsTer22