Canonical Allele Identifier: CA493300651

Gene: PAM16 CORO7-PAM16

Linked Data

• MyVariant Identifiers: chr16:g.4390945A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4340944A>C , CM000678.2:g.4340944A>C	GRCh38
NC_000016.9:g.4390945A>C , CM000678.1:g.4390945A>C	GRCh37
NC_000016.8:g.4330946A>C	NCBI36
NG_016391.1:g.13721A>C
NG_016391.2:g.31184A>C
NG_054893.1:g.15429T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318059.8:c.267T>G (PAM16) MANE Select	ENSP00000315693.3:p.Gly89=
ENST00000318059.7:c.267T>G (PAM16)	ENSP00000315693.3:p.Gly89=
ENST00000571178.1:c.241T>G (PAM16)
ENST00000571941.5:c.327T>G (PAM16)	ENSP00000460708.1:p.Gly109=
ENST00000571986.5:c.*160T>G (PAM16)	ENSP00000459802.1:n.*160T>G
ENST00000572274.1:n.669T>G (CORO7-PAM16)
ENST00000572467.5:c.3036T>G (CORO7-PAM16)	ENSP00000460885.1:p.Gly1012=
ENST00000573236.5:n.523T>G (PAM16)
ENST00000573450.5:n.400T>G (PAM16)
ENST00000573553.5:c.327T>G (PAM16)	ENSP00000459955.1:p.Gly109=
ENST00000573614.5:n.471T>G (PAM16)
ENST00000575334.5:c.*1562T>G (CORO7-PAM16)	ENSP00000458607.1:n.*1562T>G
ENST00000575636.5:c.*160T>G (PAM16)	ENSP00000458914.1:n.*160T>G
ENST00000575848.5:c.303T>G (PAM16)	ENSP00000458412.1:p.Gly101=
ENST00000576217.1:c.267T>G (PAM16)	ENSP00000461047.1:p.Gly89=
ENST00000577031.5:c.267T>G (PAM16)	ENSP00000459113.1:p.Gly89=
NM_001201479.1:c.3036T>G (CORO7-PAM16)	NP_001188408.1:p.Gly1012=
NM_016069.9:c.267T>G (PAM16)	NP_057153.8:p.Gly89=
NM_016069.10:c.267T>G (PAM16)	NP_057153.8:p.Gly89=
NM_016069.11:c.267T>G (PAM16) MANE Select	NP_057153.8:p.Gly89=
NM_001201479.2:c.3036T>G (CORO7-PAM16)	NP_001188408.1:p.Gly1012=