Canonical Allele Identifier: CA493300655

Gene: PAM16 CORO7-PAM16

Linked Data

• MyVariant Identifiers: chr16:g.4390948C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4340947C>G , CM000678.2:g.4340947C>G	GRCh38
NC_000016.9:g.4390948C>G , CM000678.1:g.4390948C>G	GRCh37
NC_000016.8:g.4330949C>G	NCBI36
NG_016391.1:g.13724C>G
NG_016391.2:g.31187C>G
NG_054893.1:g.15426G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318059.8:c.264G>C (PAM16) MANE Select	ENSP00000315693.3:p.Val88=
ENST00000318059.7:c.264G>C (PAM16)	ENSP00000315693.3:p.Val88=
ENST00000571178.1:c.238G>C (PAM16)
ENST00000571941.5:c.324G>C (PAM16)	ENSP00000460708.1:p.Val108=
ENST00000571986.5:c.*157G>C (PAM16)	ENSP00000459802.1:n.*157G>C
ENST00000572274.1:n.666G>C (CORO7-PAM16)
ENST00000572467.5:c.3033G>C (CORO7-PAM16)	ENSP00000460885.1:p.Val1011=
ENST00000573236.5:n.520G>C (PAM16)
ENST00000573450.5:n.397G>C (PAM16)
ENST00000573553.5:c.324G>C (PAM16)	ENSP00000459955.1:p.Val108=
ENST00000573614.5:n.468G>C (PAM16)
ENST00000575334.5:c.*1559G>C (CORO7-PAM16)	ENSP00000458607.1:n.*1559G>C
ENST00000575636.5:c.*157G>C (PAM16)	ENSP00000458914.1:n.*157G>C
ENST00000575848.5:c.300G>C (PAM16)	ENSP00000458412.1:p.Val100=
ENST00000576217.1:c.264G>C (PAM16)	ENSP00000461047.1:p.Val88=
ENST00000577031.5:c.264G>C (PAM16)	ENSP00000459113.1:p.Val88=
NM_001201479.1:c.3033G>C (CORO7-PAM16)	NP_001188408.1:p.Val1011=
NM_016069.9:c.264G>C (PAM16)	NP_057153.8:p.Val88=
NM_016069.10:c.264G>C (PAM16)	NP_057153.8:p.Val88=
NM_016069.11:c.264G>C (PAM16) MANE Select	NP_057153.8:p.Val88=
NM_001201479.2:c.3033G>C (CORO7-PAM16)	NP_001188408.1:p.Val1011=