Canonical Allele Identifier: CA2843586464

Gene: PAM16 CORO7-PAM16

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4340821_4340822insG , CM000678.2:g.4340821_4340822insG	GRCh38
NC_000016.9:g.4390822_4390823insG , CM000678.1:g.4390822_4390823insG	GRCh37
NC_000016.8:g.4330823_4330824insG	NCBI36
NG_016391.1:g.13598_13599insG
NG_016391.2:g.31061_31062insG
NG_054893.1:g.15551_15552insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318059.8:c.291+98_291+99insC (PAM16) MANE Select	ENSP00000315693.3:n.291+98_291+99insC
ENST00000318059.7:c.291+98_291+99insC (PAM16)	ENSP00000315693.3:n.291+98_291+99insC
ENST00000571178.1:c.265+98_265+99insC (PAM16)
ENST00000571941.5:c.351+98_351+99insC (PAM16)	ENSP00000460708.1:n.351+98_351+99insC
ENST00000571986.5:c.*184+98_*184+99insC (PAM16)	ENSP00000459802.1:n.*184+98_*184+99insC
ENST00000572467.5:c.3060+98_3060+99insC (CORO7-PAM16)	ENSP00000460885.1:n.3060+98_3060+99insC
ENST00000573236.5:n.547+98_547+99insC (PAM16)
ENST00000573450.5:n.424+98_424+99insC (PAM16)
ENST00000573553.5:c.351+98_351+99insC (PAM16)	ENSP00000459955.1:n.351+98_351+99insC
ENST00000573614.5:n.495+98_495+99insC (PAM16)
ENST00000575334.5:c.*1586+98_*1586+99insC (CORO7-PAM16)	ENSP00000458607.1:n.*1586+98_*1586+99insC
ENST00000575636.5:c.*184+98_*184+99insC (PAM16)	ENSP00000458914.1:n.*184+98_*184+99insC
ENST00000575848.5:c.327+98_327+99insC (PAM16)	ENSP00000458412.1:n.327+98_327+99insC
ENST00000576217.1:c.291+98_291+99insC (PAM16)	ENSP00000461047.1:n.291+98_291+99insC
ENST00000577031.5:c.291+98_291+99insC (PAM16)	ENSP00000459113.1:n.291+98_291+99insC
NM_001201479.1:c.3060+98_3060+99insC (CORO7-PAM16)	NP_001188408.1:n.3060+98_3060+99insC
NM_016069.9:c.291+98_291+99insC (PAM16)	NP_057153.8:n.291+98_291+99insC
NM_016069.10:c.291+98_291+99insC (PAM16)	NP_057153.8:n.291+98_291+99insC
NM_016069.11:c.291+98_291+99insC (PAM16) MANE Select	NP_057153.8:n.291+98_291+99insC
NM_001201479.2:c.3060+98_3060+99insC (CORO7-PAM16)	NP_001188408.1:n.3060+98_3060+99insC