Canonical Allele Identifier: CA2203260901

Gene: PAM16 CORO7-PAM16

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4340981T= , CM000678.2:g.4340981T=	GRCh38
NC_000016.9:g.4390982T= , CM000678.1:g.4390982T=	GRCh37
NC_000016.8:g.4330983T=	NCBI36
NG_016391.1:g.13758T=
NG_016391.2:g.31221T=
NG_054893.1:g.15392A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318059.8:c.230A= (PAM16) MANE Select	ENSP00000315693.3:p.Tyr77=
ENST00000318059.7:c.230A= (PAM16)	ENSP00000315693.3:p.Tyr77=
ENST00000571178.1:c.204A= (PAM16)
ENST00000571941.5:c.290A= (PAM16)	ENSP00000460708.1:p.Tyr97=
ENST00000571986.5:c.*123A= (PAM16)	ENSP00000459802.1:n.*123A=
ENST00000572274.1:n.632A= (CORO7-PAM16)
ENST00000572467.5:c.2999A= (CORO7-PAM16)	ENSP00000460885.1:p.Tyr1000=
ENST00000573236.5:n.486A= (PAM16)
ENST00000573450.5:n.363A= (PAM16)
ENST00000573553.5:c.290A= (PAM16)	ENSP00000459955.1:p.Tyr97=
ENST00000573614.5:n.434A= (PAM16)
ENST00000575334.5:c.*1525A= (CORO7-PAM16)	ENSP00000458607.1:n.*1525A=
ENST00000575636.5:c.*123A= (PAM16)	ENSP00000458914.1:n.*123A=
ENST00000575848.5:c.266A= (PAM16)	ENSP00000458412.1:p.Tyr89=
ENST00000576217.1:c.230A= (PAM16)	ENSP00000461047.1:p.Tyr77=
ENST00000577031.5:c.230A= (PAM16)	ENSP00000459113.1:p.Tyr77=
NM_001201479.1:c.2999A= (CORO7-PAM16)	NP_001188408.1:p.Tyr1000=
NM_016069.9:c.230A= (PAM16)	NP_057153.8:p.Tyr77=
NM_016069.10:c.230A= (PAM16)	NP_057153.8:p.Tyr77=
NM_016069.11:c.230A= (PAM16) MANE Select	NP_057153.8:p.Tyr77=
NM_001201479.2:c.2999A= (CORO7-PAM16)	NP_001188408.1:p.Tyr1000=