Canonical Allele Identifier: CA2203260892

Gene: PAM16 CORO7-PAM16

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4340969A= , CM000678.2:g.4340969A=	GRCh38
NC_000016.9:g.4390970A= , CM000678.1:g.4390970A=	GRCh37
NC_000016.8:g.4330971A=	NCBI36
NG_016391.1:g.13746A=
NG_016391.2:g.31209A=
NG_054893.1:g.15404T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318059.8:c.242T= (PAM16) MANE Select	ENSP00000315693.3:p.Phe81=
ENST00000318059.7:c.242T= (PAM16)	ENSP00000315693.3:p.Phe81=
ENST00000571178.1:c.216T= (PAM16)
ENST00000571941.5:c.302T= (PAM16)	ENSP00000460708.1:p.Phe101=
ENST00000571986.5:c.*135T= (PAM16)	ENSP00000459802.1:n.*135T=
ENST00000572274.1:n.644T= (CORO7-PAM16)
ENST00000572467.5:c.3011T= (CORO7-PAM16)	ENSP00000460885.1:p.Phe1004=
ENST00000573236.5:n.498T= (PAM16)
ENST00000573450.5:n.375T= (PAM16)
ENST00000573553.5:c.302T= (PAM16)	ENSP00000459955.1:p.Phe101=
ENST00000573614.5:n.446T= (PAM16)
ENST00000575334.5:c.*1537T= (CORO7-PAM16)	ENSP00000458607.1:n.*1537T=
ENST00000575636.5:c.*135T= (PAM16)	ENSP00000458914.1:n.*135T=
ENST00000575848.5:c.278T= (PAM16)	ENSP00000458412.1:p.Phe93=
ENST00000576217.1:c.242T= (PAM16)	ENSP00000461047.1:p.Phe81=
ENST00000577031.5:c.242T= (PAM16)	ENSP00000459113.1:p.Phe81=
NM_001201479.1:c.3011T= (CORO7-PAM16)	NP_001188408.1:p.Phe1004=
NM_016069.9:c.242T= (PAM16)	NP_057153.8:p.Phe81=
NM_016069.10:c.242T= (PAM16)	NP_057153.8:p.Phe81=
NM_016069.11:c.242T= (PAM16) MANE Select	NP_057153.8:p.Phe81=
NM_001201479.2:c.3011T= (CORO7-PAM16)	NP_001188408.1:p.Phe1004=