Canonical Allele Identifier: CA394602737

Gene: PAM16 CORO7-PAM16

Linked Data

• MyVariant Identifiers: chr16:g.4390959C>A (hg19) ; chr16:g.4340958C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4340958C>A , CM000678.2:g.4340958C>A	GRCh38
NC_000016.9:g.4390959C>A , CM000678.1:g.4390959C>A	GRCh37
NC_000016.8:g.4330960C>A	NCBI36
NG_016391.1:g.13735C>A
NG_016391.2:g.31198C>A
NG_054893.1:g.15415G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318059.8:c.253G>T (PAM16) MANE Select	ENSP00000315693.3:p.Asp85Tyr
ENST00000318059.7:c.253G>T (PAM16)	ENSP00000315693.3:p.Asp85Tyr
ENST00000571178.1:c.227G>T (PAM16)
ENST00000571941.5:c.313G>T (PAM16)	ENSP00000460708.1:p.Asp105Tyr
ENST00000571986.5:c.*146G>T (PAM16)	ENSP00000459802.1:n.*146G>T
ENST00000572274.1:n.655G>T (CORO7-PAM16)
ENST00000572467.5:c.3022G>T (CORO7-PAM16)	ENSP00000460885.1:p.Asp1008Tyr
ENST00000573236.5:n.509G>T (PAM16)
ENST00000573450.5:n.386G>T (PAM16)
ENST00000573553.5:c.313G>T (PAM16)	ENSP00000459955.1:p.Asp105Tyr
ENST00000573614.5:n.457G>T (PAM16)
ENST00000575334.5:c.*1548G>T (CORO7-PAM16)	ENSP00000458607.1:n.*1548G>T
ENST00000575636.5:c.*146G>T (PAM16)	ENSP00000458914.1:n.*146G>T
ENST00000575848.5:c.289G>T (PAM16)	ENSP00000458412.1:p.Asp97Tyr
ENST00000576217.1:c.253G>T (PAM16)	ENSP00000461047.1:p.Asp85Tyr
ENST00000577031.5:c.253G>T (PAM16)	ENSP00000459113.1:p.Asp85Tyr
NM_001201479.1:c.3022G>T (CORO7-PAM16)	NP_001188408.1:p.Asp1008Tyr
NM_016069.9:c.253G>T (PAM16)	NP_057153.8:p.Asp85Tyr
NM_016069.10:c.253G>T (PAM16)	NP_057153.8:p.Asp85Tyr
NM_016069.11:c.253G>T (PAM16) MANE Select	NP_057153.8:p.Asp85Tyr
NM_001201479.2:c.3022G>T (CORO7-PAM16)	NP_001188408.1:p.Asp1008Tyr