Canonical Allele Identifier: CA493300638

Gene: PAM16 CORO7-PAM16

Linked Data

• MyVariant Identifiers: chr16:g.4390927C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4340926C>T , CM000678.2:g.4340926C>T	GRCh38
NC_000016.9:g.4390927C>T , CM000678.1:g.4390927C>T	GRCh37
NC_000016.8:g.4330928C>T	NCBI36
NG_016391.1:g.13703C>T
NG_016391.2:g.31166C>T
NG_054893.1:g.15447G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318059.8:c.285G>A (PAM16) MANE Select	ENSP00000315693.3:p.Gln95=
ENST00000318059.7:c.285G>A (PAM16)	ENSP00000315693.3:p.Gln95=
ENST00000571178.1:c.259G>A (PAM16)
ENST00000571941.5:c.345G>A (PAM16)	ENSP00000460708.1:p.Gln115=
ENST00000571986.5:c.*178G>A (PAM16)	ENSP00000459802.1:n.*178G>A
ENST00000572467.5:c.3054G>A (CORO7-PAM16)	ENSP00000460885.1:p.Gln1018=
ENST00000573236.5:n.541G>A (PAM16)
ENST00000573450.5:n.418G>A (PAM16)
ENST00000573553.5:c.345G>A (PAM16)	ENSP00000459955.1:p.Gln115=
ENST00000573614.5:n.489G>A (PAM16)
ENST00000575334.5:c.*1580G>A (CORO7-PAM16)	ENSP00000458607.1:n.*1580G>A
ENST00000575636.5:c.*178G>A (PAM16)	ENSP00000458914.1:n.*178G>A
ENST00000575848.5:c.321G>A (PAM16)	ENSP00000458412.1:p.Gln107=
ENST00000576217.1:c.285G>A (PAM16)	ENSP00000461047.1:p.Gln95=
ENST00000577031.5:c.285G>A (PAM16)	ENSP00000459113.1:p.Gln95=
NM_001201479.1:c.3054G>A (CORO7-PAM16)	NP_001188408.1:p.Gln1018=
NM_016069.9:c.285G>A (PAM16)	NP_057153.8:p.Gln95=
NM_016069.10:c.285G>A (PAM16)	NP_057153.8:p.Gln95=
NM_016069.11:c.285G>A (PAM16) MANE Select	NP_057153.8:p.Gln95=
NM_001201479.2:c.3054G>A (CORO7-PAM16)	NP_001188408.1:p.Gln1018=