Canonical Allele Identifier: CA394602724
Gene: PAM16 HGNC NCBI
CORO7-PAM16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.4340955T>C , CM000678.2:g.4340955T>C GRCh38
NC_000016.9:g.4390956T>C , CM000678.1:g.4390956T>C GRCh37
NC_000016.8:g.4330957T>C NCBI36
NG_016391.1:g.13732T>C
NG_016391.2:g.31195T>C
NG_054893.1:g.15418A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000318059.8:c.256A>G (PAM16) MANE Select ENSP00000315693.3:p.Lys86Glu
ENST00000318059.7:c.256A>G (PAM16) ENSP00000315693.3:p.Lys86Glu
ENST00000571178.1:c.230A>G (PAM16)
ENST00000571941.5:c.316A>G (PAM16) ENSP00000460708.1:p.Lys106Glu
ENST00000571986.5:c.*149A>G (PAM16) ENSP00000459802.1:n.*149A>G
ENST00000572274.1:n.658A>G (CORO7-PAM16)
ENST00000572467.5:c.3025A>G (CORO7-PAM16) ENSP00000460885.1:p.Lys1009Glu
ENST00000573236.5:n.512A>G (PAM16)
ENST00000573450.5:n.389A>G (PAM16)
ENST00000573553.5:c.316A>G (PAM16) ENSP00000459955.1:p.Lys106Glu
ENST00000573614.5:n.460A>G (PAM16)
ENST00000575334.5:c.*1551A>G (CORO7-PAM16) ENSP00000458607.1:n.*1551A>G
ENST00000575636.5:c.*149A>G (PAM16) ENSP00000458914.1:n.*149A>G
ENST00000575848.5:c.292A>G (PAM16) ENSP00000458412.1:p.Lys98Glu
ENST00000576217.1:c.256A>G (PAM16) ENSP00000461047.1:p.Lys86Glu
ENST00000577031.5:c.256A>G (PAM16) ENSP00000459113.1:p.Lys86Glu
NM_001201479.1:c.3025A>G (CORO7-PAM16) NP_001188408.1:p.Lys1009Glu
NM_016069.9:c.256A>G (PAM16) NP_057153.8:p.Lys86Glu
NM_016069.10:c.256A>G (PAM16) NP_057153.8:p.Lys86Glu
NM_016069.11:c.256A>G (PAM16) MANE Select NP_057153.8:p.Lys86Glu
NM_001201479.2:c.3025A>G (CORO7-PAM16) NP_001188408.1:p.Lys1009Glu