Canonical Allele Identifier: CA394602817

Gene: PAM16 CORO7-PAM16

Linked Data

• MyVariant Identifiers: chr16:g.4390977G>C (hg19) ; chr16:g.4340976G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4340976G>C , CM000678.2:g.4340976G>C	GRCh38
NC_000016.9:g.4390977G>C , CM000678.1:g.4390977G>C	GRCh37
NC_000016.8:g.4330978G>C	NCBI36
NG_016391.1:g.13753G>C
NG_016391.2:g.31216G>C
NG_054893.1:g.15397C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318059.8:c.235C>G (PAM16) MANE Select	ENSP00000315693.3:p.His79Asp
ENST00000318059.7:c.235C>G (PAM16)	ENSP00000315693.3:p.His79Asp
ENST00000571178.1:c.209C>G (PAM16)
ENST00000571941.5:c.295C>G (PAM16)	ENSP00000460708.1:p.His99Asp
ENST00000571986.5:c.*128C>G (PAM16)	ENSP00000459802.1:n.*128C>G
ENST00000572274.1:n.637C>G (CORO7-PAM16)
ENST00000572467.5:c.3004C>G (CORO7-PAM16)	ENSP00000460885.1:p.His1002Asp
ENST00000573236.5:n.491C>G (PAM16)
ENST00000573450.5:n.368C>G (PAM16)
ENST00000573553.5:c.295C>G (PAM16)	ENSP00000459955.1:p.His99Asp
ENST00000573614.5:n.439C>G (PAM16)
ENST00000575334.5:c.*1530C>G (CORO7-PAM16)	ENSP00000458607.1:n.*1530C>G
ENST00000575636.5:c.*128C>G (PAM16)	ENSP00000458914.1:n.*128C>G
ENST00000575848.5:c.271C>G (PAM16)	ENSP00000458412.1:p.His91Asp
ENST00000576217.1:c.235C>G (PAM16)	ENSP00000461047.1:p.His79Asp
ENST00000577031.5:c.235C>G (PAM16)	ENSP00000459113.1:p.His79Asp
NM_001201479.1:c.3004C>G (CORO7-PAM16)	NP_001188408.1:p.His1002Asp
NM_016069.9:c.235C>G (PAM16)	NP_057153.8:p.His79Asp
NM_016069.10:c.235C>G (PAM16)	NP_057153.8:p.His79Asp
NM_016069.11:c.235C>G (PAM16) MANE Select	NP_057153.8:p.His79Asp
NM_001201479.2:c.3004C>G (CORO7-PAM16)	NP_001188408.1:p.His1002Asp