Canonical Allele Identifier: CA1884347425

Gene: TPRN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137192179_137192183delinsAAGTG , CM000671.2:g.137192179_137192183delinsAAGTG	GRCh38
NC_000009.11:g.140086631_140086635delinsAAGTG , CM000671.1:g.140086631_140086635delinsAAGTG	GRCh37
NC_000009.10:g.139206452_139206456delinsAAGTG	NCBI36
NG_027801.1:g.13529_13533delinsCACTT
NG_027801.2:g.17011_17015delinsCACTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409012.6:c.2074-9_2074-5delinsCACTT MANE Select	ENSP00000387100.4:n.2074-9_2074-5delinsCACTT
ENST00000333046.8:c.1543_1547delinsCACTT	ENSP00000327617.4:p.His515=
ENST00000409012.4:c.2074-9_2074-5delinsCACTT	ENSP00000387100.4:n.2074-9_2074-5delinsCACTT
ENST00000477345.1:n.2795-9_2795-5delinsCACTT
NM_001128228.2:c.2074-9_2074-5delinsCACTT	NP_001121700.2:n.2074-9_2074-5delinsCACTT
NM_001128228.3:c.2074-9_2074-5delinsCACTT MANE Select	NP_001121700.2:n.2074-9_2074-5delinsCACTT