Canonical Allele Identifier: CA2326045260

Gene: INSL3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17818099_17818104delinsCCACTT , CM000681.2:g.17818099_17818104delinsCCACTT	GRCh38
NC_000019.9:g.17928908_17928913delinsCCACTT , CM000681.1:g.17928908_17928913delinsCCACTT	GRCh37
NC_000019.8:g.17789908_17789913delinsCCACTT	NCBI36
NG_012092.1:g.8408_8413delinsAAGTGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000317306.8:c.191-1045_191-1040delinsAAGTGG MANE Select	ENSP00000321724.6:n.191-1045_191-1040delinsAAGTGG
ENST00000317306.7:c.191-1045_191-1040delinsAAGTGG	ENSP00000321724.6:n.191-1045_191-1040delinsAAGTGG
ENST00000379695.5:c.286-1045_286-1040delinsAAGTGG	ENSP00000369017.4:n.286-1045_286-1040delinsAAGTGG
ENST00000598577.1:c.190-1023_190-1018delinsAAGTGG
NM_001265587.1:c.286-1045_286-1040delinsAAGTGG	NP_001252516.1:n.286-1045_286-1040delinsAAGTGG
NM_005543.3:c.191-1045_191-1040delinsAAGTGG	NP_005534.2:n.191-1045_191-1040delinsAAGTGG
NM_001265587.2:c.286-1045_286-1040delinsAAGTGG	NP_001252516.1:n.286-1045_286-1040delinsAAGTGG
NM_005543.4:c.191-1045_191-1040delinsAAGTGG MANE Select	NP_005534.2:n.191-1045_191-1040delinsAAGTGG