Canonical Allele Identifier: CA493300660

Gene: PAM16 CORO7-PAM16

Linked Data

• MyVariant Identifiers: chr16:g.4390960A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4340959A>G , CM000678.2:g.4340959A>G	GRCh38
NC_000016.9:g.4390960A>G , CM000678.1:g.4390960A>G	GRCh37
NC_000016.8:g.4330961A>G	NCBI36
NG_016391.1:g.13736A>G
NG_016391.2:g.31199A>G
NG_054893.1:g.15414T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318059.8:c.252T>C (PAM16) MANE Select	ENSP00000315693.3:p.Asn84=
ENST00000318059.7:c.252T>C (PAM16)	ENSP00000315693.3:p.Asn84=
ENST00000571178.1:c.226T>C (PAM16)
ENST00000571941.5:c.312T>C (PAM16)	ENSP00000460708.1:p.Asn104=
ENST00000571986.5:c.*145T>C (PAM16)	ENSP00000459802.1:n.*145T>C
ENST00000572274.1:n.654T>C (CORO7-PAM16)
ENST00000572467.5:c.3021T>C (CORO7-PAM16)	ENSP00000460885.1:p.Asn1007=
ENST00000573236.5:n.508T>C (PAM16)
ENST00000573450.5:n.385T>C (PAM16)
ENST00000573553.5:c.312T>C (PAM16)	ENSP00000459955.1:p.Asn104=
ENST00000573614.5:n.456T>C (PAM16)
ENST00000575334.5:c.*1547T>C (CORO7-PAM16)	ENSP00000458607.1:n.*1547T>C
ENST00000575636.5:c.*145T>C (PAM16)	ENSP00000458914.1:n.*145T>C
ENST00000575848.5:c.288T>C (PAM16)	ENSP00000458412.1:p.Asn96=
ENST00000576217.1:c.252T>C (PAM16)	ENSP00000461047.1:p.Asn84=
ENST00000577031.5:c.252T>C (PAM16)	ENSP00000459113.1:p.Asn84=
NM_001201479.1:c.3021T>C (CORO7-PAM16)	NP_001188408.1:p.Asn1007=
NM_016069.9:c.252T>C (PAM16)	NP_057153.8:p.Asn84=
NM_016069.10:c.252T>C (PAM16)	NP_057153.8:p.Asn84=
NM_016069.11:c.252T>C (PAM16) MANE Select	NP_057153.8:p.Asn84=
NM_001201479.2:c.3021T>C (CORO7-PAM16)	NP_001188408.1:p.Asn1007=